id
stringlengths 15
19
| document_id
stringlengths 15
19
| passages
list | entities
list | events
list | coreferences
list | relations
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|---|---|---|---|---|---|---|
split_0_train_4700
|
split_0_train_4700
|
[
{
"id": "split_0_train_4700_passage",
"type": "progene_text",
"text": [
"Removal of A antigen with alpha-N-acetylgalactosaminidase or B antigen with alpha-galactosidase did not affect its multimer size or antigenic level , but decreased the ristocetin cofactor ( RCoF ) activity of the respective VWF by 33 - 39 % ( P < 0.01 - 0.002 ) ."
],
"offsets": [
[
0,
263
]
]
}
] |
[
{
"id": "split_0_train_7412_entity",
"type": "progene_text",
"text": [
"alpha-N-acetylgalactosaminidase"
],
"offsets": [
[
26,
57
]
],
"normalized": []
},
{
"id": "split_0_train_7413_entity",
"type": "progene_text",
"text": [
"alpha-galactosidase"
],
"offsets": [
[
76,
95
]
],
"normalized": []
},
{
"id": "split_0_train_7414_entity",
"type": "progene_text",
"text": [
"VWF"
],
"offsets": [
[
224,
227
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4701
|
split_0_train_4701
|
[
{
"id": "split_0_train_4701_passage",
"type": "progene_text",
"text": [
"Removal of A or B antigen from VWF did not affect the binding of the VWF to immobilized type III collagen ."
],
"offsets": [
[
0,
107
]
]
}
] |
[
{
"id": "split_0_train_7415_entity",
"type": "progene_text",
"text": [
"VWF"
],
"offsets": [
[
31,
34
]
],
"normalized": []
},
{
"id": "split_0_train_7416_entity",
"type": "progene_text",
"text": [
"VWF"
],
"offsets": [
[
69,
72
]
],
"normalized": []
},
{
"id": "split_0_train_7417_entity",
"type": "progene_text",
"text": [
"type III collagen"
],
"offsets": [
[
88,
105
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4702
|
split_0_train_4702
|
[
{
"id": "split_0_train_4702_passage",
"type": "progene_text",
"text": [
"A and B antigens were not detected in platelet VWF ."
],
"offsets": [
[
0,
52
]
]
}
] |
[
{
"id": "split_0_train_7418_entity",
"type": "progene_text",
"text": [
"VWF"
],
"offsets": [
[
47,
50
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4703
|
split_0_train_4703
|
[
{
"id": "split_0_train_4703_passage",
"type": "progene_text",
"text": [
"These results indicate that AB structures play a role in platelet aggregating activity of VWF ."
],
"offsets": [
[
0,
95
]
]
}
] |
[
{
"id": "split_0_train_7419_entity",
"type": "progene_text",
"text": [
"VWF"
],
"offsets": [
[
90,
93
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4704
|
split_0_train_4704
|
[
{
"id": "split_0_train_4704_passage",
"type": "progene_text",
"text": [
"ApoE polymorphism and fish oil supplementation in subjects with an atherogenic lipoprotein phenotype ."
],
"offsets": [
[
0,
102
]
]
}
] |
[
{
"id": "split_0_train_7420_entity",
"type": "progene_text",
"text": [
"ApoE"
],
"offsets": [
[
0,
4
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4705
|
split_0_train_4705
|
[
{
"id": "split_0_train_4705_passage",
"type": "progene_text",
"text": [
"The study assessed the efficacy of fish oil supplementation in counteracting the classic dyslipidemia of the atherogenic lipoprotein phenotype ( ALP ) ."
],
"offsets": [
[
0,
152
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_4706
|
split_0_train_4706
|
[
{
"id": "split_0_train_4706_passage",
"type": "progene_text",
"text": [
"In addition , the impact of the common apolipoprotein E ( apoE ) polymorphism on the fasting and postprandial lipid profile and on responsiveness to the dietary intervention was established ."
],
"offsets": [
[
0,
191
]
]
}
] |
[
{
"id": "split_0_train_7421_entity",
"type": "progene_text",
"text": [
"apolipoprotein E"
],
"offsets": [
[
39,
55
]
],
"normalized": []
},
{
"id": "split_0_train_7422_entity",
"type": "progene_text",
"text": [
"apoE"
],
"offsets": [
[
58,
62
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4707
|
split_0_train_4707
|
[
{
"id": "split_0_train_4707_passage",
"type": "progene_text",
"text": [
"Fifty - five ALP males ( aged 34 to 69 years , body mass index 22 to 35 kg / m(2) , triglyceride [ TG ] levels 1.5 to 4.0 mmol / L , high density lipoprotein cholesterol [ HDL - C ] < 1.1 mmol / l , and percent low density lipoprotein [LDL]-3 > 40 % total LDL ) completed a randomized placebo - controlled crossover trial of fish oil ( 3.0 g eicosapentaenoic acid / docosahexaenoic acid per day ) and placebo ( olive oil ) capsules with the 6 - week treatment arms separated by a 12 - week washout period ."
],
"offsets": [
[
0,
506
]
]
}
] |
[
{
"id": "split_0_train_7423_entity",
"type": "progene_text",
"text": [
"high density lipoprotein"
],
"offsets": [
[
133,
157
]
],
"normalized": []
},
{
"id": "split_0_train_7424_entity",
"type": "progene_text",
"text": [
"HDL"
],
"offsets": [
[
172,
175
]
],
"normalized": []
},
{
"id": "split_0_train_7425_entity",
"type": "progene_text",
"text": [
"low density lipoprotein [LDL]-3"
],
"offsets": [
[
211,
242
]
],
"normalized": []
},
{
"id": "split_0_train_7426_entity",
"type": "progene_text",
"text": [
"LDL"
],
"offsets": [
[
256,
259
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4708
|
split_0_train_4708
|
[
{
"id": "split_0_train_4708_passage",
"type": "progene_text",
"text": [
"In addition to fasting blood samples , at the end of each intervention arm , a postprandial assessment of lipid metabolism was carried out ."
],
"offsets": [
[
0,
140
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_4709
|
split_0_train_4709
|
[
{
"id": "split_0_train_4709_passage",
"type": "progene_text",
"text": [
"Fish oil supplementation resulted in a reduction in fasting TG level of 35 % ( P < 0.001 ) , in postprandial TG response of 26 % ( TG area under the curve , P < 0.001 ) , and in percent LDL-3 of 26 % ( P < 0.05 ) ."
],
"offsets": [
[
0,
214
]
]
}
] |
[
{
"id": "split_0_train_7427_entity",
"type": "progene_text",
"text": [
"LDL-3"
],
"offsets": [
[
186,
191
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4710
|
split_0_train_4710
|
[
{
"id": "split_0_train_4710_passage",
"type": "progene_text",
"text": [
"However , no change in HDL - C levels was evident ( P = 0.752 ) ."
],
"offsets": [
[
0,
65
]
]
}
] |
[
{
"id": "split_0_train_7428_entity",
"type": "progene_text",
"text": [
"HDL"
],
"offsets": [
[
23,
26
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4711
|
split_0_train_4711
|
[
{
"id": "split_0_train_4711_passage",
"type": "progene_text",
"text": [
"ANCOVA showed that baseline HDL - C levels were significantly lower in apoE4 carriers ( P = 0.035 ) ."
],
"offsets": [
[
0,
101
]
]
}
] |
[
{
"id": "split_0_train_7429_entity",
"type": "progene_text",
"text": [
"HDL"
],
"offsets": [
[
28,
31
]
],
"normalized": []
},
{
"id": "split_0_train_7430_entity",
"type": "progene_text",
"text": [
"apoE4"
],
"offsets": [
[
71,
76
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4712
|
split_0_train_4712
|
[
{
"id": "split_0_train_4712_passage",
"type": "progene_text",
"text": [
"The apoE genotype also had a striking impact on lipid responses to fish oil intervention ."
],
"offsets": [
[
0,
90
]
]
}
] |
[
{
"id": "split_0_train_7431_entity",
"type": "progene_text",
"text": [
"apoE"
],
"offsets": [
[
4,
8
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4713
|
split_0_train_4713
|
[
{
"id": "split_0_train_4713_passage",
"type": "progene_text",
"text": [
"Individuals with an apoE2 allele displayed a marked reduction in postprandial incremental TG response ( TG incremental area under the curve , P = 0.023 ) and a trend toward an increase in lipoprotein lipase activity relative to non - E2 carriers ."
],
"offsets": [
[
0,
247
]
]
}
] |
[
{
"id": "split_0_train_7432_entity",
"type": "progene_text",
"text": [
"apoE2"
],
"offsets": [
[
20,
25
]
],
"normalized": []
},
{
"id": "split_0_train_7433_entity",
"type": "progene_text",
"text": [
"lipoprotein lipase"
],
"offsets": [
[
188,
206
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4714
|
split_0_train_4714
|
[
{
"id": "split_0_train_4714_passage",
"type": "progene_text",
"text": [
"In apoE4 individuals , a significant increase in total cholesterol and a trend toward a reduction in HDL - C relative to the common homozygous E3 / E3 profile was evident ."
],
"offsets": [
[
0,
172
]
]
}
] |
[
{
"id": "split_0_train_7434_entity",
"type": "progene_text",
"text": [
"apoE4"
],
"offsets": [
[
3,
8
]
],
"normalized": []
},
{
"id": "split_0_train_7435_entity",
"type": "progene_text",
"text": [
"HDL"
],
"offsets": [
[
101,
104
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4715
|
split_0_train_4715
|
[
{
"id": "split_0_train_4715_passage",
"type": "progene_text",
"text": [
"Our data demonstrate the efficacy of fish oil fatty acids in counteracting the proatherogenic lipid profile of the ALP but also that the apoE genotype influences responsiveness to this dietary treatment ."
],
"offsets": [
[
0,
204
]
]
}
] |
[
{
"id": "split_0_train_7436_entity",
"type": "progene_text",
"text": [
"apoE"
],
"offsets": [
[
137,
141
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4716
|
split_0_train_4716
|
[
{
"id": "split_0_train_4716_passage",
"type": "progene_text",
"text": [
"The impact of the ovulatory cycle on cytokine production : evaluation of systemic , cervicovaginal , and salivary compartments ."
],
"offsets": [
[
0,
128
]
]
}
] |
[
{
"id": "split_0_train_7437_entity",
"type": "progene_text",
"text": [
"cytokine"
],
"offsets": [
[
37,
45
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4717
|
split_0_train_4717
|
[
{
"id": "split_0_train_4717_passage",
"type": "progene_text",
"text": [
"To understand the impact of the menstrual cycle on immunologic parameters , we measured the level of cytokines and chemokines from plasma , cervicovaginal lavage ( CVL ) , and saliva samples of 6 premenopausal women during the follicular and luteal phases of the ovulatory cycle ."
],
"offsets": [
[
0,
280
]
]
}
] |
[
{
"id": "split_0_train_7438_entity",
"type": "progene_text",
"text": [
"cytokines"
],
"offsets": [
[
101,
110
]
],
"normalized": []
},
{
"id": "split_0_train_7439_entity",
"type": "progene_text",
"text": [
"chemokines"
],
"offsets": [
[
115,
125
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4718
|
split_0_train_4718
|
[
{
"id": "split_0_train_4718_passage",
"type": "progene_text",
"text": [
"We demonstrate that the level of plasma interleukin-8 ( IL-8 ) was 4 - fold higher during the follicular phase than the luteal phase ( p = 0.004 ) , whereas plasma IL-1beta , IL-4 , IL-6 , IL-10 , interferon-gamma ( IFN-gamma ) , transforming growth factor - beta ( TGF-beta ) , tumor necrosis factor - alpha ( TNF-alpha ) , macrophage inflammatory protein-1alpha ( MIP-1alpha ) , and TNF receptor II ( TNFR II ) were not altered during the ovulatory cycle ."
],
"offsets": [
[
0,
458
]
]
}
] |
[
{
"id": "split_0_train_7440_entity",
"type": "progene_text",
"text": [
"interleukin-8"
],
"offsets": [
[
40,
53
]
],
"normalized": []
},
{
"id": "split_0_train_7441_entity",
"type": "progene_text",
"text": [
"IL-8"
],
"offsets": [
[
56,
60
]
],
"normalized": []
},
{
"id": "split_0_train_7442_entity",
"type": "progene_text",
"text": [
"IL-1beta"
],
"offsets": [
[
164,
172
]
],
"normalized": []
},
{
"id": "split_0_train_7443_entity",
"type": "progene_text",
"text": [
"IL-4"
],
"offsets": [
[
175,
179
]
],
"normalized": []
},
{
"id": "split_0_train_7444_entity",
"type": "progene_text",
"text": [
"IL-6"
],
"offsets": [
[
182,
186
]
],
"normalized": []
},
{
"id": "split_0_train_7445_entity",
"type": "progene_text",
"text": [
"IL-10"
],
"offsets": [
[
189,
194
]
],
"normalized": []
},
{
"id": "split_0_train_7446_entity",
"type": "progene_text",
"text": [
"interferon-gamma"
],
"offsets": [
[
197,
213
]
],
"normalized": []
},
{
"id": "split_0_train_7447_entity",
"type": "progene_text",
"text": [
"IFN-gamma"
],
"offsets": [
[
216,
225
]
],
"normalized": []
},
{
"id": "split_0_train_7448_entity",
"type": "progene_text",
"text": [
"transforming growth factor - beta"
],
"offsets": [
[
230,
263
]
],
"normalized": []
},
{
"id": "split_0_train_7449_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
266,
274
]
],
"normalized": []
},
{
"id": "split_0_train_7450_entity",
"type": "progene_text",
"text": [
"tumor necrosis factor - alpha"
],
"offsets": [
[
279,
308
]
],
"normalized": []
},
{
"id": "split_0_train_7451_entity",
"type": "progene_text",
"text": [
"TNF-alpha"
],
"offsets": [
[
311,
320
]
],
"normalized": []
},
{
"id": "split_0_train_7452_entity",
"type": "progene_text",
"text": [
"macrophage inflammatory protein-1alpha"
],
"offsets": [
[
325,
363
]
],
"normalized": []
},
{
"id": "split_0_train_7453_entity",
"type": "progene_text",
"text": [
"MIP-1alpha"
],
"offsets": [
[
366,
376
]
],
"normalized": []
},
{
"id": "split_0_train_7454_entity",
"type": "progene_text",
"text": [
"TNF receptor II"
],
"offsets": [
[
385,
400
]
],
"normalized": []
},
{
"id": "split_0_train_7455_entity",
"type": "progene_text",
"text": [
"TNFR II"
],
"offsets": [
[
403,
410
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4719
|
split_0_train_4719
|
[
{
"id": "split_0_train_4719_passage",
"type": "progene_text",
"text": [
"In the vaginal compartment , as measured from CVL samples , the levels of IL-6 and IL-1beta were both 5 - fold higher in the follicular than the luteal phase ( p = 0.0002 and 0.03 , respectively ) ."
],
"offsets": [
[
0,
198
]
]
}
] |
[
{
"id": "split_0_train_7456_entity",
"type": "progene_text",
"text": [
"IL-6"
],
"offsets": [
[
74,
78
]
],
"normalized": []
},
{
"id": "split_0_train_7457_entity",
"type": "progene_text",
"text": [
"IL-1beta"
],
"offsets": [
[
83,
91
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4720
|
split_0_train_4720
|
[
{
"id": "split_0_train_4720_passage",
"type": "progene_text",
"text": [
"Salivary cytokine and chemokine samples were similar when measured during the luteal and the follicular phases ."
],
"offsets": [
[
0,
112
]
]
}
] |
[
{
"id": "split_0_train_7458_entity",
"type": "progene_text",
"text": [
"cytokine"
],
"offsets": [
[
9,
17
]
],
"normalized": []
},
{
"id": "split_0_train_7459_entity",
"type": "progene_text",
"text": [
"chemokine"
],
"offsets": [
[
22,
31
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4721
|
split_0_train_4721
|
[
{
"id": "split_0_train_4721_passage",
"type": "progene_text",
"text": [
"Additional analysis of lymphocyte subsets for phenotypic and functional markers indicated that they were not influenced by the ovulatory cycle ."
],
"offsets": [
[
0,
144
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_4722
|
split_0_train_4722
|
[
{
"id": "split_0_train_4722_passage",
"type": "progene_text",
"text": [
"Collectively , these data suggest that IL-6 , IL-8 , and IL-1beta are differentially regulated during the ovulatory cycle ."
],
"offsets": [
[
0,
123
]
]
}
] |
[
{
"id": "split_0_train_7460_entity",
"type": "progene_text",
"text": [
"IL-6"
],
"offsets": [
[
39,
43
]
],
"normalized": []
},
{
"id": "split_0_train_7461_entity",
"type": "progene_text",
"text": [
"IL-8"
],
"offsets": [
[
46,
50
]
],
"normalized": []
},
{
"id": "split_0_train_7462_entity",
"type": "progene_text",
"text": [
"IL-1beta"
],
"offsets": [
[
57,
65
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4723
|
split_0_train_4723
|
[
{
"id": "split_0_train_4723_passage",
"type": "progene_text",
"text": [
"Identification of a common receptor for three types of rat cytokine - induced neutrophil chemoattractants ( CINCs ) ."
],
"offsets": [
[
0,
117
]
]
}
] |
[
{
"id": "split_0_train_7463_entity",
"type": "progene_text",
"text": [
"cytokine - induced neutrophil chemoattractants"
],
"offsets": [
[
59,
105
]
],
"normalized": []
},
{
"id": "split_0_train_7464_entity",
"type": "progene_text",
"text": [
"CINCs"
],
"offsets": [
[
108,
113
]
],
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}
] |
[] |
[] |
[] |
split_0_train_4724
|
split_0_train_4724
|
[
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"id": "split_0_train_4724_passage",
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"Rat cytokine - induced neutrophil chemoattractant-1 ( CINC-1 ) , CINC-2 and CINC-3 / macrophage inflammatory protein-2 ( MIP-2 ) , members of the CXC chemokine family , are potent chemotactic factors for neutrophils ."
],
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0,
217
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]
}
] |
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{
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"type": "progene_text",
"text": [
"CXC chemokine family"
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[
146,
166
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],
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}
] |
[] |
[] |
[] |
split_0_train_4725
|
split_0_train_4725
|
[
{
"id": "split_0_train_4725_passage",
"type": "progene_text",
"text": [
"In order to identify the receptor for CINCs , rat CXC chemokine receptor 2 ( CXCR2 ) was cloned and expressed in HEK293 cells ."
],
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[
0,
127
]
]
}
] |
[
{
"id": "split_0_train_7472_entity",
"type": "progene_text",
"text": [
"CINCs"
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38,
43
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{
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{
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"text": [
"CXCR2"
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77,
82
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],
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}
] |
[] |
[] |
[] |
split_0_train_4726
|
split_0_train_4726
|
[
{
"id": "split_0_train_4726_passage",
"type": "progene_text",
"text": [
"CINC-1 , CINC-2 and CINC-3 induced calcium mobilizations dose - dependently in CXCR2 - transfected cells , whereas formyl-methionyl-leucyl-phenylalanine ( FMLP ) did not ."
],
"offsets": [
[
0,
171
]
]
}
] |
[
{
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0,
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{
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{
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"type": "progene_text",
"text": [
"CXCR2"
],
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[
79,
84
]
],
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}
] |
[] |
[] |
[] |
split_0_train_4727
|
split_0_train_4727
|
[
{
"id": "split_0_train_4727_passage",
"type": "progene_text",
"text": [
"CINC-3 induced enhancement of cytoplasmic calcium concentration more potently than CINC-1 and CINC-2 , and desensitized calcium transients induced by CINC-1 and CINC-2 , which were essentially identical to those observed in rat neutrophils ."
],
"offsets": [
[
0,
241
]
]
}
] |
[
{
"id": "split_0_train_7479_entity",
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0,
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{
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83,
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{
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{
"id": "split_0_train_7482_entity",
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150,
156
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{
"id": "split_0_train_7483_entity",
"type": "progene_text",
"text": [
"CINC-2"
],
"offsets": [
[
161,
167
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4728
|
split_0_train_4728
|
[
{
"id": "split_0_train_4728_passage",
"type": "progene_text",
"text": [
"In addition , anti - CXCR2 serum inhibited neutrophil chemotactic activities of three types of CINCs almost completely ."
],
"offsets": [
[
0,
120
]
]
}
] |
[
{
"id": "split_0_train_7484_entity",
"type": "progene_text",
"text": [
"CXCR2"
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21,
26
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},
{
"id": "split_0_train_7485_entity",
"type": "progene_text",
"text": [
"CINCs"
],
"offsets": [
[
95,
100
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4729
|
split_0_train_4729
|
[
{
"id": "split_0_train_4729_passage",
"type": "progene_text",
"text": [
"The mutant CINC-3 , whose amino - terminal amino acid sequence ( SELR ) was replaced to AAR , lost chemotactic activity of its own but inhibited that of CINC-1 and CINC-2 potently , and that of CINC-3 weakly ."
],
"offsets": [
[
0,
209
]
]
}
] |
[
{
"id": "split_0_train_7486_entity",
"type": "progene_text",
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"CINC-3"
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11,
17
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{
"id": "split_0_train_7487_entity",
"type": "progene_text",
"text": [
"CINC-1"
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153,
159
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{
"id": "split_0_train_7488_entity",
"type": "progene_text",
"text": [
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164,
170
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{
"id": "split_0_train_7489_entity",
"type": "progene_text",
"text": [
"CINC-3"
],
"offsets": [
[
194,
200
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4730
|
split_0_train_4730
|
[
{
"id": "split_0_train_4730_passage",
"type": "progene_text",
"text": [
"The results indicate that rat CXCR2 on neutrophils is the unique receptor for all three types of CINCs , and CINC-1 / - 2 and CINC-3 exert different biological activities through the common receptor ."
],
"offsets": [
[
0,
200
]
]
}
] |
[
{
"id": "split_0_train_7490_entity",
"type": "progene_text",
"text": [
"CXCR2"
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30,
35
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{
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"type": "progene_text",
"text": [
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97,
102
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},
{
"id": "split_0_train_7492_entity",
"type": "progene_text",
"text": [
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109,
121
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{
"id": "split_0_train_7493_entity",
"type": "progene_text",
"text": [
"CINC-3"
],
"offsets": [
[
126,
132
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4731
|
split_0_train_4731
|
[
{
"id": "split_0_train_4731_passage",
"type": "progene_text",
"text": [
"ASD4 , a new GATA factor of Neurospora crassa , displays sequence - specific DNA binding and functions in ascus and ascospore development ."
],
"offsets": [
[
0,
139
]
]
}
] |
[
{
"id": "split_0_train_7494_entity",
"type": "progene_text",
"text": [
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0,
4
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},
{
"id": "split_0_train_7495_entity",
"type": "progene_text",
"text": [
"GATA factor"
],
"offsets": [
[
13,
24
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4732
|
split_0_train_4732
|
[
{
"id": "split_0_train_4732_passage",
"type": "progene_text",
"text": [
"A new gene encoding a novel GATA factor , ASD4 , of Neurospora crassa was isolated and demonstrated to possess one intron and to specify an open reading frame encoding a protein with 427 amino acid residues ."
],
"offsets": [
[
0,
208
]
]
}
] |
[
{
"id": "split_0_train_7496_entity",
"type": "progene_text",
"text": [
"GATA factor"
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[
28,
39
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{
"id": "split_0_train_7497_entity",
"type": "progene_text",
"text": [
"ASD4"
],
"offsets": [
[
42,
46
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4733
|
split_0_train_4733
|
[
{
"id": "split_0_train_4733_passage",
"type": "progene_text",
"text": [
"The ASD4 protein contains a single GATA - type zinc finger and a putative coiled - coil domain ."
],
"offsets": [
[
0,
96
]
]
}
] |
[
{
"id": "split_0_train_7498_entity",
"type": "progene_text",
"text": [
"ASD4"
],
"offsets": [
[
4,
8
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4734
|
split_0_train_4734
|
[
{
"id": "split_0_train_4734_passage",
"type": "progene_text",
"text": [
"Unlike related proteins , DAL80 in yeast and NREB in Penicillium , ASD4 does not appear to be involved in regulation of nitrogen metabolism ."
],
"offsets": [
[
0,
141
]
]
}
] |
[
{
"id": "split_0_train_7499_entity",
"type": "progene_text",
"text": [
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26,
31
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},
{
"id": "split_0_train_7500_entity",
"type": "progene_text",
"text": [
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45,
49
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},
{
"id": "split_0_train_7501_entity",
"type": "progene_text",
"text": [
"ASD4"
],
"offsets": [
[
67,
71
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4735
|
split_0_train_4735
|
[
{
"id": "split_0_train_4735_passage",
"type": "progene_text",
"text": [
"An Asd-4 null mutant obtained by the rip procedure did not show any effect upon nitrogen control , but instead resulted in severe defects in ascus and ascospore genesis ."
],
"offsets": [
[
0,
170
]
]
}
] |
[
{
"id": "split_0_train_7502_entity",
"type": "progene_text",
"text": [
"Asd-4"
],
"offsets": [
[
3,
8
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4736
|
split_0_train_4736
|
[
{
"id": "split_0_train_4736_passage",
"type": "progene_text",
"text": [
"The Asd-4 rip mutant is dominant to Asd-4 + ."
],
"offsets": [
[
0,
45
]
]
}
] |
[
{
"id": "split_0_train_7503_entity",
"type": "progene_text",
"text": [
"Asd-4"
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[
4,
9
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],
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},
{
"id": "split_0_train_7504_entity",
"type": "progene_text",
"text": [
"Asd-4"
],
"offsets": [
[
36,
41
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4737
|
split_0_train_4737
|
[
{
"id": "split_0_train_4737_passage",
"type": "progene_text",
"text": [
"A cross of the Asd-4 mutant with wild - type resulted in fruiting bodies that appeared to be normal macroscopically but which were complete devoid of asci and ascospores ."
],
"offsets": [
[
0,
171
]
]
}
] |
[
{
"id": "split_0_train_7505_entity",
"type": "progene_text",
"text": [
"Asd-4"
],
"offsets": [
[
15,
20
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4738
|
split_0_train_4738
|
[
{
"id": "split_0_train_4738_passage",
"type": "progene_text",
"text": [
"Introduction of the Asd-4 + gene into the Asd-4 rip mutant corrected the defect in ascus and ascospore development in crosses with wild - type ."
],
"offsets": [
[
0,
144
]
]
}
] |
[
{
"id": "split_0_train_7506_entity",
"type": "progene_text",
"text": [
"Asd-4"
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"offsets": [
[
20,
25
]
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},
{
"id": "split_0_train_7507_entity",
"type": "progene_text",
"text": [
"Asd-4"
],
"offsets": [
[
42,
47
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4739
|
split_0_train_4739
|
[
{
"id": "split_0_train_4739_passage",
"type": "progene_text",
"text": [
"Mobility shift assays demonstrated that ASD4 acts as a sequence - specific DNA binding protein and recognizes DNA fragments that contain GATA core elements ."
],
"offsets": [
[
0,
157
]
]
}
] |
[
{
"id": "split_0_train_7508_entity",
"type": "progene_text",
"text": [
"ASD4"
],
"offsets": [
[
40,
44
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4740
|
split_0_train_4740
|
[
{
"id": "split_0_train_4740_passage",
"type": "progene_text",
"text": [
"Gel filtration and cross - linking experiments revealed that the ASD4 protein exists as a tetramer in solution ."
],
"offsets": [
[
0,
112
]
]
}
] |
[
{
"id": "split_0_train_7509_entity",
"type": "progene_text",
"text": [
"ASD4"
],
"offsets": [
[
65,
69
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4741
|
split_0_train_4741
|
[
{
"id": "split_0_train_4741_passage",
"type": "progene_text",
"text": [
"These results suggest that the ASD4 protein functions positively as a transcriptional regulator of sexual development in Neurospora ."
],
"offsets": [
[
0,
133
]
]
}
] |
[
{
"id": "split_0_train_7510_entity",
"type": "progene_text",
"text": [
"ASD4"
],
"offsets": [
[
31,
35
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4742
|
split_0_train_4742
|
[
{
"id": "split_0_train_4742_passage",
"type": "progene_text",
"text": [
"Expression of the ftsY gene , encoding a homologue of the alpha subunit of mammalian signal recognition particle receptor , is controlled by different promoters in vegetative and sporulating cells of Bacillus subtilis ."
],
"offsets": [
[
0,
219
]
]
}
] |
[
{
"id": "split_0_train_7511_entity",
"type": "progene_text",
"text": [
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18,
22
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{
"id": "split_0_train_7512_entity",
"type": "progene_text",
"text": [
"signal recognition particle receptor"
],
"offsets": [
[
85,
121
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4743
|
split_0_train_4743
|
[
{
"id": "split_0_train_4743_passage",
"type": "progene_text",
"text": [
"Bacillus subtilis FtsY ( Srb ) is a homologue of the alpha subunit of the receptor for mammalian signal - recognition particle ( SRP ) and is essential for protein secretion and vegetative cell growth ."
],
"offsets": [
[
0,
202
]
]
}
] |
[
{
"id": "split_0_train_7513_entity",
"type": "progene_text",
"text": [
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18,
22
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},
{
"id": "split_0_train_7514_entity",
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"text": [
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25,
28
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},
{
"id": "split_0_train_7515_entity",
"type": "progene_text",
"text": [
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97,
126
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},
{
"id": "split_0_train_7516_entity",
"type": "progene_text",
"text": [
"SRP"
],
"offsets": [
[
129,
132
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4744
|
split_0_train_4744
|
[
{
"id": "split_0_train_4744_passage",
"type": "progene_text",
"text": [
"The ftsY gene is expressed during both the exponential phase and sporulation ."
],
"offsets": [
[
0,
78
]
]
}
] |
[
{
"id": "split_0_train_7517_entity",
"type": "progene_text",
"text": [
"ftsY"
],
"offsets": [
[
4,
8
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4745
|
split_0_train_4745
|
[
{
"id": "split_0_train_4745_passage",
"type": "progene_text",
"text": [
"In vegetative cells , ftsY is transcribed with two upstream genes , rncS and smc , that are under the control of the major transcription factor sigma ( A ) ."
],
"offsets": [
[
0,
157
]
]
}
] |
[
{
"id": "split_0_train_7518_entity",
"type": "progene_text",
"text": [
"ftsY"
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22,
26
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},
{
"id": "split_0_train_7519_entity",
"type": "progene_text",
"text": [
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68,
72
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{
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"text": [
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77,
80
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{
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"type": "progene_text",
"text": [
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123,
143
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},
{
"id": "split_0_train_7522_entity",
"type": "progene_text",
"text": [
"sigma ( A )"
],
"offsets": [
[
144,
155
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4746
|
split_0_train_4746
|
[
{
"id": "split_0_train_4746_passage",
"type": "progene_text",
"text": [
"During sporulation , Northern hybridization detected ftsY mRNA in wild - type cells , but not in sporulating cells of sigma ( K ) and gerE mutants ."
],
"offsets": [
[
0,
148
]
]
}
] |
[
{
"id": "split_0_train_7523_entity",
"type": "progene_text",
"text": [
"ftsY"
],
"offsets": [
[
53,
57
]
],
"normalized": []
},
{
"id": "split_0_train_7524_entity",
"type": "progene_text",
"text": [
"sigma ( K )"
],
"offsets": [
[
118,
129
]
],
"normalized": []
},
{
"id": "split_0_train_7525_entity",
"type": "progene_text",
"text": [
"gerE"
],
"offsets": [
[
134,
138
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4747
|
split_0_train_4747
|
[
{
"id": "split_0_train_4747_passage",
"type": "progene_text",
"text": [
"Therefore , ftsY is solely expressed during sporulation from a sigma ( K ) - and GerE - controlled promoter that is located immediately upstream of ftsY inside the smc gene ."
],
"offsets": [
[
0,
174
]
]
}
] |
[
{
"id": "split_0_train_7526_entity",
"type": "progene_text",
"text": [
"ftsY"
],
"offsets": [
[
12,
16
]
],
"normalized": []
},
{
"id": "split_0_train_7527_entity",
"type": "progene_text",
"text": [
"sigma ( K )"
],
"offsets": [
[
63,
74
]
],
"normalized": []
},
{
"id": "split_0_train_7528_entity",
"type": "progene_text",
"text": [
"GerE"
],
"offsets": [
[
81,
85
]
],
"normalized": []
},
{
"id": "split_0_train_7529_entity",
"type": "progene_text",
"text": [
"ftsY"
],
"offsets": [
[
148,
152
]
],
"normalized": []
},
{
"id": "split_0_train_7530_entity",
"type": "progene_text",
"text": [
"smc"
],
"offsets": [
[
164,
167
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4748
|
split_0_train_4748
|
[
{
"id": "split_0_train_4748_passage",
"type": "progene_text",
"text": [
"To examine the role of FtsY during sporulation , the B. subtilis strain ISR39 was constructed , a ftsY conditional mutant in which ftsY expression can be shut off during spore formation but not during the vegetative state ."
],
"offsets": [
[
0,
223
]
]
}
] |
[
{
"id": "split_0_train_7531_entity",
"type": "progene_text",
"text": [
"FtsY"
],
"offsets": [
[
23,
27
]
],
"normalized": []
},
{
"id": "split_0_train_7532_entity",
"type": "progene_text",
"text": [
"ftsY"
],
"offsets": [
[
98,
102
]
],
"normalized": []
},
{
"id": "split_0_train_7533_entity",
"type": "progene_text",
"text": [
"ftsY"
],
"offsets": [
[
131,
135
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4749
|
split_0_train_4749
|
[
{
"id": "split_0_train_4749_passage",
"type": "progene_text",
"text": [
"Electron microscopy showed that the outer coat of ISR39 spores was not completely assembled and immunoelectron microscopy localized FtsY to the inner and outer coats of wild - type spores ."
],
"offsets": [
[
0,
189
]
]
}
] |
[
{
"id": "split_0_train_7534_entity",
"type": "progene_text",
"text": [
"FtsY"
],
"offsets": [
[
132,
136
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4750
|
split_0_train_4750
|
[
{
"id": "split_0_train_4750_passage",
"type": "progene_text",
"text": [
"Inhalation of toluene diisocyanate affects cytochrome P450 2B1 expression in rat lung ."
],
"offsets": [
[
0,
87
]
]
}
] |
[
{
"id": "split_0_train_7535_entity",
"type": "progene_text",
"text": [
"cytochrome P450 2B1"
],
"offsets": [
[
43,
62
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4751
|
split_0_train_4751
|
[
{
"id": "split_0_train_4751_passage",
"type": "progene_text",
"text": [
"In the lung the expression of xenobiotic - metabolizing enzymes such as cytochromes P450 ( CYP ) and glutathione S-transferases ( GST ) may be affected by inhaled pollutants ."
],
"offsets": [
[
0,
175
]
]
}
] |
[
{
"id": "split_0_train_7536_entity",
"type": "progene_text",
"text": [
"cytochromes P450"
],
"offsets": [
[
72,
88
]
],
"normalized": []
},
{
"id": "split_0_train_7537_entity",
"type": "progene_text",
"text": [
"CYP"
],
"offsets": [
[
91,
94
]
],
"normalized": []
},
{
"id": "split_0_train_7538_entity",
"type": "progene_text",
"text": [
"glutathione S-transferases"
],
"offsets": [
[
101,
127
]
],
"normalized": []
},
{
"id": "split_0_train_7539_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
130,
133
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4752
|
split_0_train_4752
|
[
{
"id": "split_0_train_4752_passage",
"type": "progene_text",
"text": [
"Toluene diisocyanate ( TDI ) is a highly volatile chemical compound known to induce a wide array of diseases in workers exposed to vapors or sprays , including respiratory allergy and asthma ."
],
"offsets": [
[
0,
192
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_4753
|
split_0_train_4753
|
[
{
"id": "split_0_train_4753_passage",
"type": "progene_text",
"text": [
"We investigated the effect of inhaled TDI on expression of CYP 1A1 , 2B1 , 2E1 , and 3A1 and of alpha - , mu - , and pi-GST in rat lung ."
],
"offsets": [
[
0,
137
]
]
}
] |
[
{
"id": "split_0_train_7540_entity",
"type": "progene_text",
"text": [
"CYP 1A1 , 2B1 , 2E1 , and 3A1"
],
"offsets": [
[
59,
88
]
],
"normalized": []
},
{
"id": "split_0_train_7541_entity",
"type": "progene_text",
"text": [
"alpha - , mu - , and pi-GST"
],
"offsets": [
[
96,
123
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4754
|
split_0_train_4754
|
[
{
"id": "split_0_train_4754_passage",
"type": "progene_text",
"text": [
"Animals were exposed to targeted concentrations of 0.01 , 0.1 , or 1 ppm TDI vapors or to cleaned filtered air for 8 h ."
],
"offsets": [
[
0,
120
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_4755
|
split_0_train_4755
|
[
{
"id": "split_0_train_4755_passage",
"type": "progene_text",
"text": [
"Expression of CYP and GST was analyzed 18 24 h after the end of exposure using western blotting , northern blotting , and immunohistochemistry ."
],
"offsets": [
[
0,
144
]
]
}
] |
[
{
"id": "split_0_train_7542_entity",
"type": "progene_text",
"text": [
"CYP"
],
"offsets": [
[
14,
17
]
],
"normalized": []
},
{
"id": "split_0_train_7543_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
22,
25
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4756
|
split_0_train_4756
|
[
{
"id": "split_0_train_4756_passage",
"type": "progene_text",
"text": [
"Constitutive levels of CYP 2B1 and 3A1 proteins were found in lung tissue from control rats , whereas CYP 1A1 and 2E1 proteins were not detectable ."
],
"offsets": [
[
0,
148
]
]
}
] |
[
{
"id": "split_0_train_7544_entity",
"type": "progene_text",
"text": [
"CYP 2B1 and 3A1"
],
"offsets": [
[
23,
38
]
],
"normalized": []
},
{
"id": "split_0_train_7545_entity",
"type": "progene_text",
"text": [
"CYP 1A1 and 2E1"
],
"offsets": [
[
102,
117
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4757
|
split_0_train_4757
|
[
{
"id": "split_0_train_4757_passage",
"type": "progene_text",
"text": [
"Animal exposure to TDI vapors neither modified CYP 3A1 protein expression , nor led to any detectable expression of CYP 1A1 or 2E1 ."
],
"offsets": [
[
0,
132
]
]
}
] |
[
{
"id": "split_0_train_7546_entity",
"type": "progene_text",
"text": [
"CYP 3A1"
],
"offsets": [
[
47,
54
]
],
"normalized": []
},
{
"id": "split_0_train_7547_entity",
"type": "progene_text",
"text": [
"CYP 1A1 or 2E1"
],
"offsets": [
[
116,
130
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4758
|
split_0_train_4758
|
[
{
"id": "split_0_train_4758_passage",
"type": "progene_text",
"text": [
"In contrast , exposure to 1 ppm TDI induced a 40 % reduction in CYP 2B1 protein levels ."
],
"offsets": [
[
0,
88
]
]
}
] |
[
{
"id": "split_0_train_7548_entity",
"type": "progene_text",
"text": [
"CYP 2B1"
],
"offsets": [
[
64,
71
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4759
|
split_0_train_4759
|
[
{
"id": "split_0_train_4759_passage",
"type": "progene_text",
"text": [
"This decrease was associated with a 33 % decrease in CYP 2B1 mRNA levels ."
],
"offsets": [
[
0,
74
]
]
}
] |
[
{
"id": "split_0_train_7549_entity",
"type": "progene_text",
"text": [
"CYP 2B1"
],
"offsets": [
[
53,
60
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4760
|
split_0_train_4760
|
[
{
"id": "split_0_train_4760_passage",
"type": "progene_text",
"text": [
"Additionally , CYP 2B1 immunolabeling localized to ciliated epithelial cells , Clara cells , and type II alveolar cells in the lung tissue of control rats was markedly decreased in animals exposed to 1 ppm TDI ."
],
"offsets": [
[
0,
211
]
]
}
] |
[
{
"id": "split_0_train_7550_entity",
"type": "progene_text",
"text": [
"CYP 2B1"
],
"offsets": [
[
15,
22
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4761
|
split_0_train_4761
|
[
{
"id": "split_0_train_4761_passage",
"type": "progene_text",
"text": [
"Constitutive levels of alpha - , mu - , and pi - GST proteins were found in lung tissue from control rats ."
],
"offsets": [
[
0,
107
]
]
}
] |
[
{
"id": "split_0_train_7551_entity",
"type": "progene_text",
"text": [
"alpha - , mu - , and pi - GST"
],
"offsets": [
[
23,
52
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4762
|
split_0_train_4762
|
[
{
"id": "split_0_train_4762_passage",
"type": "progene_text",
"text": [
"Exposure to TDI had no effect on lung expression of either of the GST ."
],
"offsets": [
[
0,
71
]
]
}
] |
[
{
"id": "split_0_train_7552_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
66,
69
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4763
|
split_0_train_4763
|
[
{
"id": "split_0_train_4763_passage",
"type": "progene_text",
"text": [
"In conclusion , this study clearly shows a selective decrease in CYP 2B1 expression by TDI vapors in rat lung ."
],
"offsets": [
[
0,
111
]
]
}
] |
[
{
"id": "split_0_train_7553_entity",
"type": "progene_text",
"text": [
"CYP 2B1"
],
"offsets": [
[
65,
72
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4764
|
split_0_train_4764
|
[
{
"id": "split_0_train_4764_passage",
"type": "progene_text",
"text": [
"The contribution of CYP 2B1 to metabolize further xenobiotics is therefore altered ."
],
"offsets": [
[
0,
84
]
]
}
] |
[
{
"id": "split_0_train_7554_entity",
"type": "progene_text",
"text": [
"CYP 2B1"
],
"offsets": [
[
20,
27
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4765
|
split_0_train_4765
|
[
{
"id": "split_0_train_4765_passage",
"type": "progene_text",
"text": [
"Molecular cloning and characterization of a cDNA and a gene for subtilisin - like serine proteases from rice ( Oryza sativa L. ) and Arabidopsis thaliana ."
],
"offsets": [
[
0,
155
]
]
}
] |
[
{
"id": "split_0_train_7555_entity",
"type": "progene_text",
"text": [
"subtilisin - like serine proteases"
],
"offsets": [
[
64,
98
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4766
|
split_0_train_4766
|
[
{
"id": "split_0_train_4766_passage",
"type": "progene_text",
"text": [
"The complete nucleotide sequences of a cDNA ( RSP1 ) that encodes a subtilisin - like serine protease ( subtilase ) of rice ( Oryza sativa L. ) and a gene ( ASP48 ) for Arabidopsis subtilase were analyzed ."
],
"offsets": [
[
0,
206
]
]
}
] |
[
{
"id": "split_0_train_7556_entity",
"type": "progene_text",
"text": [
"RSP1"
],
"offsets": [
[
46,
50
]
],
"normalized": []
},
{
"id": "split_0_train_7557_entity",
"type": "progene_text",
"text": [
"subtilisin - like serine protease"
],
"offsets": [
[
68,
101
]
],
"normalized": []
},
{
"id": "split_0_train_7558_entity",
"type": "progene_text",
"text": [
"subtilase"
],
"offsets": [
[
104,
113
]
],
"normalized": []
},
{
"id": "split_0_train_7559_entity",
"type": "progene_text",
"text": [
"ASP48"
],
"offsets": [
[
157,
162
]
],
"normalized": []
},
{
"id": "split_0_train_7560_entity",
"type": "progene_text",
"text": [
"subtilase"
],
"offsets": [
[
181,
190
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4767
|
split_0_train_4767
|
[
{
"id": "split_0_train_4767_passage",
"type": "progene_text",
"text": [
"The RSPI cDNA and ASP48 DNA encoded 736 - and 757 - residue pre - pro - polypeptides including a signal peptide with molecular masses of 78,668 Da and 79 , 414 Da , respectively ."
],
"offsets": [
[
0,
179
]
]
}
] |
[
{
"id": "split_0_train_7561_entity",
"type": "progene_text",
"text": [
"RSPI"
],
"offsets": [
[
4,
8
]
],
"normalized": []
},
{
"id": "split_0_train_7562_entity",
"type": "progene_text",
"text": [
"ASP48"
],
"offsets": [
[
18,
23
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4768
|
split_0_train_4768
|
[
{
"id": "split_0_train_4768_passage",
"type": "progene_text",
"text": [
"RSP1 is the first known serine protease in rice , and ASP48 is a gene for ara12 cDNA ."
],
"offsets": [
[
0,
86
]
]
}
] |
[
{
"id": "split_0_train_7563_entity",
"type": "progene_text",
"text": [
"RSP1"
],
"offsets": [
[
0,
4
]
],
"normalized": []
},
{
"id": "split_0_train_7564_entity",
"type": "progene_text",
"text": [
"serine protease"
],
"offsets": [
[
24,
39
]
],
"normalized": []
},
{
"id": "split_0_train_7565_entity",
"type": "progene_text",
"text": [
"ASP48"
],
"offsets": [
[
54,
59
]
],
"normalized": []
},
{
"id": "split_0_train_7566_entity",
"type": "progene_text",
"text": [
"ara12"
],
"offsets": [
[
74,
79
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4769
|
split_0_train_4769
|
[
{
"id": "split_0_train_4769_passage",
"type": "progene_text",
"text": [
"Sequence comparison and phylogenetic analysis showed that RSP1 is distantly related to all other plant subtilases and ASP48 is closely related to a tomato subtilase , SBT1 ."
],
"offsets": [
[
0,
173
]
]
}
] |
[
{
"id": "split_0_train_7567_entity",
"type": "progene_text",
"text": [
"RSP1"
],
"offsets": [
[
58,
62
]
],
"normalized": []
},
{
"id": "split_0_train_7568_entity",
"type": "progene_text",
"text": [
"subtilases"
],
"offsets": [
[
103,
113
]
],
"normalized": []
},
{
"id": "split_0_train_7569_entity",
"type": "progene_text",
"text": [
"ASP48"
],
"offsets": [
[
118,
123
]
],
"normalized": []
},
{
"id": "split_0_train_7570_entity",
"type": "progene_text",
"text": [
"subtilase"
],
"offsets": [
[
155,
164
]
],
"normalized": []
},
{
"id": "split_0_train_7571_entity",
"type": "progene_text",
"text": [
"SBT1"
],
"offsets": [
[
167,
171
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4770
|
split_0_train_4770
|
[
{
"id": "split_0_train_4770_passage",
"type": "progene_text",
"text": [
"The ASP48 gene was found to lack introns ."
],
"offsets": [
[
0,
42
]
]
}
] |
[
{
"id": "split_0_train_7572_entity",
"type": "progene_text",
"text": [
"ASP48"
],
"offsets": [
[
4,
9
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4771
|
split_0_train_4771
|
[
{
"id": "split_0_train_4771_passage",
"type": "progene_text",
"text": [
"The Arabidopsis subtilase gene appears to consist of a small gene family ."
],
"offsets": [
[
0,
74
]
]
}
] |
[
{
"id": "split_0_train_7573_entity",
"type": "progene_text",
"text": [
"subtilase"
],
"offsets": [
[
16,
25
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4772
|
split_0_train_4772
|
[
{
"id": "split_0_train_4772_passage",
"type": "progene_text",
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"The RSP1 was found to be expressed in seed and shoots of seedlings while ASP48 transcripts was found to be accumulated in immature silique and flowers , indicating that both RSP1 and ASP48 are organ - specific and may be involved in the specific proteolytic events that occur during organ development ."
],
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0,
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] |
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{
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"text": [
"ASP48"
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183,
188
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}
] |
[] |
[] |
[] |
split_0_train_4773
|
split_0_train_4773
|
[
{
"id": "split_0_train_4773_passage",
"type": "progene_text",
"text": [
"Novel G proteins , Rag C and Rag D , interact with GTP - binding proteins , Rag A and Rag B ."
],
"offsets": [
[
0,
93
]
]
}
] |
[
{
"id": "split_0_train_7578_entity",
"type": "progene_text",
"text": [
"G proteins"
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6,
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{
"id": "split_0_train_7579_entity",
"type": "progene_text",
"text": [
"Rag C"
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19,
24
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},
{
"id": "split_0_train_7580_entity",
"type": "progene_text",
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"Rag D"
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29,
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{
"id": "split_0_train_7581_entity",
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"Rag A"
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76,
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{
"id": "split_0_train_7582_entity",
"type": "progene_text",
"text": [
"Rag B"
],
"offsets": [
[
86,
91
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4774
|
split_0_train_4774
|
[
{
"id": "split_0_train_4774_passage",
"type": "progene_text",
"text": [
"Rag A / Gtr1p are G proteins and are known to be involved in the RCC1 - Ran pathway ."
],
"offsets": [
[
0,
85
]
]
}
] |
[
{
"id": "split_0_train_7583_entity",
"type": "progene_text",
"text": [
"Rag A"
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0,
5
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{
"id": "split_0_train_7584_entity",
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"text": [
"Gtr1p"
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8,
13
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{
"id": "split_0_train_7585_entity",
"type": "progene_text",
"text": [
"G proteins"
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18,
28
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{
"id": "split_0_train_7586_entity",
"type": "progene_text",
"text": [
"RCC1"
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65,
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},
{
"id": "split_0_train_7587_entity",
"type": "progene_text",
"text": [
"Ran"
],
"offsets": [
[
72,
75
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4775
|
split_0_train_4775
|
[
{
"id": "split_0_train_4775_passage",
"type": "progene_text",
"text": [
"We employed the two - hybrid method using Rag A as the bait to identify proteins binding to Rag A , and we isolated two novel human G proteins , Rag C and Rag D ."
],
"offsets": [
[
0,
162
]
]
}
] |
[
{
"id": "split_0_train_7588_entity",
"type": "progene_text",
"text": [
"Rag A"
],
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[
42,
47
]
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{
"id": "split_0_train_7589_entity",
"type": "progene_text",
"text": [
"Rag A"
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92,
97
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},
{
"id": "split_0_train_7590_entity",
"type": "progene_text",
"text": [
"G proteins"
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132,
142
]
],
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},
{
"id": "split_0_train_7591_entity",
"type": "progene_text",
"text": [
"Rag C"
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145,
150
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],
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},
{
"id": "split_0_train_7592_entity",
"type": "progene_text",
"text": [
"Rag D"
],
"offsets": [
[
155,
160
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4776
|
split_0_train_4776
|
[
{
"id": "split_0_train_4776_passage",
"type": "progene_text",
"text": [
"Rag C demonstrates homology with Rag D ( 81.1 % identity ) and with Gtr2p of Saccharomyces cerevisiae ( 46.1 % identity ) , and it belongs to the Rag A subfamily of the Ras family ."
],
"offsets": [
[
0,
181
]
]
}
] |
[
{
"id": "split_0_train_7593_entity",
"type": "progene_text",
"text": [
"Rag C"
],
"offsets": [
[
0,
5
]
],
"normalized": []
},
{
"id": "split_0_train_7594_entity",
"type": "progene_text",
"text": [
"Rag D"
],
"offsets": [
[
33,
38
]
],
"normalized": []
},
{
"id": "split_0_train_7595_entity",
"type": "progene_text",
"text": [
"Gtr2p"
],
"offsets": [
[
68,
73
]
],
"normalized": []
},
{
"id": "split_0_train_7596_entity",
"type": "progene_text",
"text": [
"Rag A subfamily"
],
"offsets": [
[
146,
161
]
],
"normalized": []
},
{
"id": "split_0_train_7597_entity",
"type": "progene_text",
"text": [
"Ras family"
],
"offsets": [
[
169,
179
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4777
|
split_0_train_4777
|
[
{
"id": "split_0_train_4777_passage",
"type": "progene_text",
"text": [
"Rag C and Rag D contain conserved GTP - binding motifs ( PM-1 , - 2 , and -3 ) in their N - terminal regions ."
],
"offsets": [
[
0,
110
]
]
}
] |
[
{
"id": "split_0_train_7598_entity",
"type": "progene_text",
"text": [
"Rag C"
],
"offsets": [
[
0,
5
]
],
"normalized": []
},
{
"id": "split_0_train_7599_entity",
"type": "progene_text",
"text": [
"Rag D"
],
"offsets": [
[
10,
15
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4778
|
split_0_train_4778
|
[
{
"id": "split_0_train_4778_passage",
"type": "progene_text",
"text": [
"Recombinant glutathione S-transferase fusion protein of Rag C efficiently bound to both [(3)H]GTP and [(3)H]GDP ."
],
"offsets": [
[
0,
113
]
]
}
] |
[
{
"id": "split_0_train_7600_entity",
"type": "progene_text",
"text": [
"glutathione S-transferase"
],
"offsets": [
[
12,
37
]
],
"normalized": []
},
{
"id": "split_0_train_7601_entity",
"type": "progene_text",
"text": [
"Rag C"
],
"offsets": [
[
56,
61
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4779
|
split_0_train_4779
|
[
{
"id": "split_0_train_4779_passage",
"type": "progene_text",
"text": [
"Rag A was associated with both Rag C and Rag D in their C - terminal regions where a potential leucine zipper motif and a coiled - coil structure were found ."
],
"offsets": [
[
0,
158
]
]
}
] |
[
{
"id": "split_0_train_7602_entity",
"type": "progene_text",
"text": [
"Rag A"
],
"offsets": [
[
0,
5
]
],
"normalized": []
},
{
"id": "split_0_train_7603_entity",
"type": "progene_text",
"text": [
"Rag C"
],
"offsets": [
[
31,
36
]
],
"normalized": []
},
{
"id": "split_0_train_7604_entity",
"type": "progene_text",
"text": [
"Rag D"
],
"offsets": [
[
41,
46
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4780
|
split_0_train_4780
|
[
{
"id": "split_0_train_4780_passage",
"type": "progene_text",
"text": [
"Rag C and D were associated with both the GDP and GTP forms of Rag A ."
],
"offsets": [
[
0,
70
]
]
}
] |
[
{
"id": "split_0_train_7605_entity",
"type": "progene_text",
"text": [
"Rag C and D"
],
"offsets": [
[
0,
11
]
],
"normalized": []
},
{
"id": "split_0_train_7606_entity",
"type": "progene_text",
"text": [
"Rag A"
],
"offsets": [
[
63,
68
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4781
|
split_0_train_4781
|
[
{
"id": "split_0_train_4781_passage",
"type": "progene_text",
"text": [
"Both Rag C and Rag D changed their subcellular localization , depending on the nucleotide - bound state of Rag A ."
],
"offsets": [
[
0,
114
]
]
}
] |
[
{
"id": "split_0_train_7607_entity",
"type": "progene_text",
"text": [
"Rag C"
],
"offsets": [
[
5,
10
]
],
"normalized": []
},
{
"id": "split_0_train_7608_entity",
"type": "progene_text",
"text": [
"Rag D"
],
"offsets": [
[
15,
20
]
],
"normalized": []
},
{
"id": "split_0_train_7609_entity",
"type": "progene_text",
"text": [
"Rag A"
],
"offsets": [
[
107,
112
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4782
|
split_0_train_4782
|
[
{
"id": "split_0_train_4782_passage",
"type": "progene_text",
"text": [
"In a similar way , the disruption of S. cerevisiae GTR1 resulted in a change in the localization of Gtr2p ."
],
"offsets": [
[
0,
107
]
]
}
] |
[
{
"id": "split_0_train_7610_entity",
"type": "progene_text",
"text": [
"GTR1"
],
"offsets": [
[
51,
55
]
],
"normalized": []
},
{
"id": "split_0_train_7611_entity",
"type": "progene_text",
"text": [
"Gtr2p"
],
"offsets": [
[
100,
105
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4783
|
split_0_train_4783
|
[
{
"id": "split_0_train_4783_passage",
"type": "progene_text",
"text": [
"Shf , a Shb - like adapter protein , is involved in PDGF-alpha-receptor regulation of apoptosis ."
],
"offsets": [
[
0,
97
]
]
}
] |
[
{
"id": "split_0_train_7612_entity",
"type": "progene_text",
"text": [
"Shf"
],
"offsets": [
[
0,
3
]
],
"normalized": []
},
{
"id": "split_0_train_7613_entity",
"type": "progene_text",
"text": [
"Shb"
],
"offsets": [
[
8,
11
]
],
"normalized": []
},
{
"id": "split_0_train_7614_entity",
"type": "progene_text",
"text": [
"adapter protein"
],
"offsets": [
[
19,
34
]
],
"normalized": []
},
{
"id": "split_0_train_7615_entity",
"type": "progene_text",
"text": [
"PDGF-alpha-receptor"
],
"offsets": [
[
52,
71
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4784
|
split_0_train_4784
|
[
{
"id": "split_0_train_4784_passage",
"type": "progene_text",
"text": [
"Recent work has implicated the importance of adapter proteins in signal transduction ."
],
"offsets": [
[
0,
86
]
]
}
] |
[
{
"id": "split_0_train_7616_entity",
"type": "progene_text",
"text": [
"adapter proteins"
],
"offsets": [
[
45,
61
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4785
|
split_0_train_4785
|
[
{
"id": "split_0_train_4785_passage",
"type": "progene_text",
"text": [
"To identify homologues of the previously identified adapter protein Shb , database searches were performed ."
],
"offsets": [
[
0,
108
]
]
}
] |
[
{
"id": "split_0_train_7617_entity",
"type": "progene_text",
"text": [
"adapter protein"
],
"offsets": [
[
52,
67
]
],
"normalized": []
},
{
"id": "split_0_train_7618_entity",
"type": "progene_text",
"text": [
"Shb"
],
"offsets": [
[
68,
71
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4786
|
split_0_train_4786
|
[
{
"id": "split_0_train_4786_passage",
"type": "progene_text",
"text": [
"A Shb - like protein was found which we have named Shf ."
],
"offsets": [
[
0,
56
]
]
}
] |
[
{
"id": "split_0_train_7619_entity",
"type": "progene_text",
"text": [
"Shb"
],
"offsets": [
[
2,
5
]
],
"normalized": []
},
{
"id": "split_0_train_7620_entity",
"type": "progene_text",
"text": [
"Shf"
],
"offsets": [
[
51,
54
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4787
|
split_0_train_4787
|
[
{
"id": "split_0_train_4787_passage",
"type": "progene_text",
"text": [
"Shf contains an SH2 domain and four putative tyrosine phosphorylation sites and is mainly expressed in skeletal muscle , brain , liver , prostate , testis , ovary , small intestine , and colon ."
],
"offsets": [
[
0,
194
]
]
}
] |
[
{
"id": "split_0_train_7621_entity",
"type": "progene_text",
"text": [
"Shf"
],
"offsets": [
[
0,
3
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4788
|
split_0_train_4788
|
[
{
"id": "split_0_train_4788_passage",
"type": "progene_text",
"text": [
"The SH2 domain of Shf bound to the PDGF-alpha - receptor at tyrosine - 720 , but not to the PDGF-beta-receptor in PAE cells ."
],
"offsets": [
[
0,
125
]
]
}
] |
[
{
"id": "split_0_train_7622_entity",
"type": "progene_text",
"text": [
"Shf"
],
"offsets": [
[
18,
21
]
],
"normalized": []
},
{
"id": "split_0_train_7623_entity",
"type": "progene_text",
"text": [
"PDGF-alpha - receptor"
],
"offsets": [
[
35,
56
]
],
"normalized": []
},
{
"id": "split_0_train_7624_entity",
"type": "progene_text",
"text": [
"PDGF-beta-receptor"
],
"offsets": [
[
92,
110
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4789
|
split_0_train_4789
|
[
{
"id": "split_0_train_4789_passage",
"type": "progene_text",
"text": [
"Pervanadate induced tyrosine phosphorylation of Shf in NIH3T3 fibroblasts overexpressing this protein , whereas PDGF-AA alone had no detectable effect ."
],
"offsets": [
[
0,
152
]
]
}
] |
[
{
"id": "split_0_train_7625_entity",
"type": "progene_text",
"text": [
"Shf"
],
"offsets": [
[
48,
51
]
],
"normalized": []
},
{
"id": "split_0_train_7626_entity",
"type": "progene_text",
"text": [
"PDGF-AA"
],
"offsets": [
[
112,
119
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4790
|
split_0_train_4790
|
[
{
"id": "split_0_train_4790_passage",
"type": "progene_text",
"text": [
"NIH3T3 cells overexpressing Shf displayed significantly lower rates of apoptosis than control cells in the presence of PDGF-AA ."
],
"offsets": [
[
0,
128
]
]
}
] |
[
{
"id": "split_0_train_7627_entity",
"type": "progene_text",
"text": [
"Shf"
],
"offsets": [
[
28,
31
]
],
"normalized": []
},
{
"id": "split_0_train_7628_entity",
"type": "progene_text",
"text": [
"PDGF-AA"
],
"offsets": [
[
119,
126
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4791
|
split_0_train_4791
|
[
{
"id": "split_0_train_4791_passage",
"type": "progene_text",
"text": [
"Our findings suggest a role for the novel adapter Shf in PDGF - receptor signaling and regulation of apoptosis ."
],
"offsets": [
[
0,
112
]
]
}
] |
[
{
"id": "split_0_train_7629_entity",
"type": "progene_text",
"text": [
"Shf"
],
"offsets": [
[
50,
53
]
],
"normalized": []
},
{
"id": "split_0_train_7630_entity",
"type": "progene_text",
"text": [
"PDGF - receptor"
],
"offsets": [
[
57,
72
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4792
|
split_0_train_4792
|
[
{
"id": "split_0_train_4792_passage",
"type": "progene_text",
"text": [
"Projection structure of the monomeric porin OmpG at 6 A resolution ."
],
"offsets": [
[
0,
68
]
]
}
] |
[
{
"id": "split_0_train_7631_entity",
"type": "progene_text",
"text": [
"porin"
],
"offsets": [
[
38,
43
]
],
"normalized": []
},
{
"id": "split_0_train_7632_entity",
"type": "progene_text",
"text": [
"OmpG"
],
"offsets": [
[
44,
48
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4793
|
split_0_train_4793
|
[
{
"id": "split_0_train_4793_passage",
"type": "progene_text",
"text": [
"The Escherichia coli porin OmpG , which acts as an efficient unspecific channel for mono - , di - and trisaccharides , has been purified and crystallized in two dimensions ."
],
"offsets": [
[
0,
173
]
]
}
] |
[
{
"id": "split_0_train_7633_entity",
"type": "progene_text",
"text": [
"porin"
],
"offsets": [
[
21,
26
]
],
"normalized": []
},
{
"id": "split_0_train_7634_entity",
"type": "progene_text",
"text": [
"OmpG"
],
"offsets": [
[
27,
31
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4794
|
split_0_train_4794
|
[
{
"id": "split_0_train_4794_passage",
"type": "progene_text",
"text": [
"Projection maps of two different crystal forms of OmpG at 6 A resolution show that the protein has a beta - barrel structure characteristic for outer membrane proteins , and that it does not form trimers , unlike most other porins such as OmpF and OmpC , but appears in monomeric form ."
],
"offsets": [
[
0,
286
]
]
}
] |
[
{
"id": "split_0_train_7635_entity",
"type": "progene_text",
"text": [
"OmpG"
],
"offsets": [
[
50,
54
]
],
"normalized": []
},
{
"id": "split_0_train_7636_entity",
"type": "progene_text",
"text": [
"porins"
],
"offsets": [
[
224,
230
]
],
"normalized": []
},
{
"id": "split_0_train_7637_entity",
"type": "progene_text",
"text": [
"OmpF"
],
"offsets": [
[
239,
243
]
],
"normalized": []
},
{
"id": "split_0_train_7638_entity",
"type": "progene_text",
"text": [
"OmpC"
],
"offsets": [
[
248,
252
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4795
|
split_0_train_4795
|
[
{
"id": "split_0_train_4795_passage",
"type": "progene_text",
"text": [
"The size of the barrel is approximately 2.5 nm , indicating that OmpG may consist of 14 beta-strands ."
],
"offsets": [
[
0,
102
]
]
}
] |
[
{
"id": "split_0_train_7639_entity",
"type": "progene_text",
"text": [
"OmpG"
],
"offsets": [
[
65,
69
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4796
|
split_0_train_4796
|
[
{
"id": "split_0_train_4796_passage",
"type": "progene_text",
"text": [
"The projection map suggests that the channel is restricted by internal loops ."
],
"offsets": [
[
0,
78
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_4797
|
split_0_train_4797
|
[
{
"id": "split_0_train_4797_passage",
"type": "progene_text",
"text": [
"CueR ( YbbI ) of Escherichia coli is a MerR family regulator controlling expression of the copper exporter CopA ."
],
"offsets": [
[
0,
113
]
]
}
] |
[
{
"id": "split_0_train_7640_entity",
"type": "progene_text",
"text": [
"CueR"
],
"offsets": [
[
0,
4
]
],
"normalized": []
},
{
"id": "split_0_train_7641_entity",
"type": "progene_text",
"text": [
"YbbI"
],
"offsets": [
[
7,
11
]
],
"normalized": []
},
{
"id": "split_0_train_7642_entity",
"type": "progene_text",
"text": [
"MerR family"
],
"offsets": [
[
39,
50
]
],
"normalized": []
},
{
"id": "split_0_train_7643_entity",
"type": "progene_text",
"text": [
"CopA"
],
"offsets": [
[
107,
111
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4798
|
split_0_train_4798
|
[
{
"id": "split_0_train_4798_passage",
"type": "progene_text",
"text": [
"We have shown that the open reading frame ybbI in the genomic sequence of Escherichia coli K-12 encodes the regulator of expression of the copper - exporting ATPase , CopA ."
],
"offsets": [
[
0,
173
]
]
}
] |
[
{
"id": "split_0_train_7644_entity",
"type": "progene_text",
"text": [
"ybbI"
],
"offsets": [
[
42,
46
]
],
"normalized": []
},
{
"id": "split_0_train_7645_entity",
"type": "progene_text",
"text": [
"ATPase"
],
"offsets": [
[
158,
164
]
],
"normalized": []
},
{
"id": "split_0_train_7646_entity",
"type": "progene_text",
"text": [
"CopA"
],
"offsets": [
[
167,
171
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_4799
|
split_0_train_4799
|
[
{
"id": "split_0_train_4799_passage",
"type": "progene_text",
"text": [
"In vivo studies showed that ybbI ( designated cueR for copper export regulator gene ) was required for copper tolerance during growth , that disruption of cueR caused loss of copA expression and that copA gene expression was regulated by cueR and by copper or silver ions ."
],
"offsets": [
[
0,
273
]
]
}
] |
[
{
"id": "split_0_train_7647_entity",
"type": "progene_text",
"text": [
"ybbI"
],
"offsets": [
[
28,
32
]
],
"normalized": []
},
{
"id": "split_0_train_7648_entity",
"type": "progene_text",
"text": [
"cueR"
],
"offsets": [
[
46,
50
]
],
"normalized": []
},
{
"id": "split_0_train_7649_entity",
"type": "progene_text",
"text": [
"copper export regulator"
],
"offsets": [
[
55,
78
]
],
"normalized": []
},
{
"id": "split_0_train_7650_entity",
"type": "progene_text",
"text": [
"cueR"
],
"offsets": [
[
155,
159
]
],
"normalized": []
},
{
"id": "split_0_train_7651_entity",
"type": "progene_text",
"text": [
"copA"
],
"offsets": [
[
175,
179
]
],
"normalized": []
},
{
"id": "split_0_train_7652_entity",
"type": "progene_text",
"text": [
"copA"
],
"offsets": [
[
200,
204
]
],
"normalized": []
},
{
"id": "split_0_train_7653_entity",
"type": "progene_text",
"text": [
"cueR"
],
"offsets": [
[
238,
242
]
],
"normalized": []
}
] |
[] |
[] |
[] |
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