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stringlengths 15
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split_0_train_5800
|
split_0_train_5800
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[
{
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"type": "progene_text",
"text": [
"These heat shock - induced foci colocalize with CREB - binding protein and heat shock factor-1 ."
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"offsets": [
[
0,
96
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]
}
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{
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"CREB - binding protein"
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48,
70
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{
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"text": [
"heat shock factor-1"
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[
75,
94
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],
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}
] |
[] |
[] |
[] |
split_0_train_5801
|
split_0_train_5801
|
[
{
"id": "split_0_train_5801_passage",
"type": "progene_text",
"text": [
"In contrast , the distribution of PDZ-RGS3 does not change during heat stress ."
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0,
79
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]
}
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[
{
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"text": [
"PDZ-RGS3"
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"offsets": [
[
34,
42
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],
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}
] |
[] |
[] |
[] |
split_0_train_5802
|
split_0_train_5802
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[
{
"id": "split_0_train_5802_passage",
"type": "progene_text",
"text": [
"When overexpressed , C2PA induces heat shock response element ( HSE ) - dependent gene transcription , whereas PDZ-RGS3 does not ."
],
"offsets": [
[
0,
130
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]
}
] |
[
{
"id": "split_0_train_8956_entity",
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"C2PA"
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21,
25
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"id": "split_0_train_8957_entity",
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"text": [
"PDZ-RGS3"
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[
111,
119
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],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5803
|
split_0_train_5803
|
[
{
"id": "split_0_train_5803_passage",
"type": "progene_text",
"text": [
"These data suggest that the function of C2PA is distinct from that of PDZ-RGS3 , and that C2PA may be involved in the heat shock response in testis ."
],
"offsets": [
[
0,
149
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]
}
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{
"id": "split_0_train_8958_entity",
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"C2PA"
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40,
44
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{
"id": "split_0_train_8959_entity",
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"PDZ-RGS3"
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70,
78
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{
"id": "split_0_train_8960_entity",
"type": "progene_text",
"text": [
"C2PA"
],
"offsets": [
[
90,
94
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5804
|
split_0_train_5804
|
[
{
"id": "split_0_train_5804_passage",
"type": "progene_text",
"text": [
"Identification of mitogen - activated protein kinase kinase as a chemoresistant pathway in MCF-7 cells by using gene expression microarray ."
],
"offsets": [
[
0,
140
]
]
}
] |
[
{
"id": "split_0_train_8961_entity",
"type": "progene_text",
"text": [
"mitogen - activated protein kinase kinase"
],
"offsets": [
[
18,
59
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5805
|
split_0_train_5805
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[
{
"id": "split_0_train_5805_passage",
"type": "progene_text",
"text": [
"BACKGROUND :"
],
"offsets": [
[
0,
12
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]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5806
|
split_0_train_5806
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[
{
"id": "split_0_train_5806_passage",
"type": "progene_text",
"text": [
"Components of the mitogen - activated protein kinase ( MAPK ) cascade have been implicated in apoptotic regulation ."
],
"offsets": [
[
0,
116
]
]
}
] |
[
{
"id": "split_0_train_8962_entity",
"type": "progene_text",
"text": [
"mitogen - activated protein kinase"
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[
18,
52
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{
"id": "split_0_train_8963_entity",
"type": "progene_text",
"text": [
"MAPK"
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"offsets": [
[
55,
59
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5807
|
split_0_train_5807
|
[
{
"id": "split_0_train_5807_passage",
"type": "progene_text",
"text": [
"This study used gene expression profiling analysis to identify and implicate mitogen - activated protein kinase kinase ( MEK5 ) - BMK1 ( big mitogen - activated kinase-1 ) / extracellular signal related protein kinase ( ERK5 ) pathway as a novel target involved in chemoresistance ."
],
"offsets": [
[
0,
282
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]
}
] |
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{
"id": "split_0_train_8964_entity",
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"mitogen - activated protein kinase kinase"
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77,
118
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{
"id": "split_0_train_8965_entity",
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"text": [
"MEK5"
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121,
125
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{
"id": "split_0_train_8966_entity",
"type": "progene_text",
"text": [
"BMK1"
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[
130,
134
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],
"normalized": []
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{
"id": "split_0_train_8967_entity",
"type": "progene_text",
"text": [
"big mitogen - activated kinase-1"
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137,
169
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{
"id": "split_0_train_8968_entity",
"type": "progene_text",
"text": [
"extracellular signal related protein kinase"
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"offsets": [
[
174,
217
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],
"normalized": []
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{
"id": "split_0_train_8969_entity",
"type": "progene_text",
"text": [
"ERK5"
],
"offsets": [
[
220,
224
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5808
|
split_0_train_5808
|
[
{
"id": "split_0_train_5808_passage",
"type": "progene_text",
"text": [
"METHODS :"
],
"offsets": [
[
0,
9
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5809
|
split_0_train_5809
|
[
{
"id": "split_0_train_5809_passage",
"type": "progene_text",
"text": [
"Differential gene expression between apoptotically sensitive ( APO+) and apoptotically resistant ( APO-) MCF-7 cell variants was determined by using microarray and confirmed by reverse transcriptase - polymerase chain reaction ( RT - PCR ) ."
],
"offsets": [
[
0,
241
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5810
|
split_0_train_5810
|
[
{
"id": "split_0_train_5810_passage",
"type": "progene_text",
"text": [
"An apoptotic / viability reporter gene assay was used to deter - mine the effects of the transfection of a dominant - negative mutant of BMK1 ( BMK1 / DN ) in conjunction with apoptotic - inducing agents ( etoposide , tumor necrosis factor - alpha [ TNF ] , or TNF - related apoptosis - inducing ligand [ TRAIL ] ) , with or without phorbol ester ( PMA ) ."
],
"offsets": [
[
0,
356
]
]
}
] |
[
{
"id": "split_0_train_8970_entity",
"type": "progene_text",
"text": [
"BMK1"
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"offsets": [
[
137,
141
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],
"normalized": []
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{
"id": "split_0_train_8971_entity",
"type": "progene_text",
"text": [
"BMK1"
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144,
148
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],
"normalized": []
},
{
"id": "split_0_train_8972_entity",
"type": "progene_text",
"text": [
"tumor necrosis factor - alpha"
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218,
247
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],
"normalized": []
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{
"id": "split_0_train_8973_entity",
"type": "progene_text",
"text": [
"TNF"
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"offsets": [
[
250,
253
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],
"normalized": []
},
{
"id": "split_0_train_8974_entity",
"type": "progene_text",
"text": [
"TNF - related apoptosis - inducing ligand"
],
"offsets": [
[
261,
302
]
],
"normalized": []
},
{
"id": "split_0_train_8975_entity",
"type": "progene_text",
"text": [
"TRAIL"
],
"offsets": [
[
305,
310
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5811
|
split_0_train_5811
|
[
{
"id": "split_0_train_5811_passage",
"type": "progene_text",
"text": [
"RESULTS :"
],
"offsets": [
[
0,
9
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5812
|
split_0_train_5812
|
[
{
"id": "split_0_train_5812_passage",
"type": "progene_text",
"text": [
"Of the 1186 genes detected through microarray analysis , MEK5 was increased 22 - fold in APO - cells ."
],
"offsets": [
[
0,
102
]
]
}
] |
[
{
"id": "split_0_train_8976_entity",
"type": "progene_text",
"text": [
"MEK5"
],
"offsets": [
[
57,
61
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5813
|
split_0_train_5813
|
[
{
"id": "split_0_train_5813_passage",
"type": "progene_text",
"text": [
"Overexpression of MEK5 was confirmed by using RT - PCR analysis ."
],
"offsets": [
[
0,
65
]
]
}
] |
[
{
"id": "split_0_train_8977_entity",
"type": "progene_text",
"text": [
"MEK5"
],
"offsets": [
[
18,
22
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5814
|
split_0_train_5814
|
[
{
"id": "split_0_train_5814_passage",
"type": "progene_text",
"text": [
"Expression of BMK1 / DN alone resulted in a dose - dependent increase in cell death versus control ( P < .05 ) ."
],
"offsets": [
[
0,
112
]
]
}
] |
[
{
"id": "split_0_train_8978_entity",
"type": "progene_text",
"text": [
"BMK1"
],
"offsets": [
[
14,
18
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5815
|
split_0_train_5815
|
[
{
"id": "split_0_train_5815_passage",
"type": "progene_text",
"text": [
"In addition , BMK1 / DN enhanced the sensitivity of MCF-7 cells to treatment - induced cell death ( P < .05 ) ."
],
"offsets": [
[
0,
111
]
]
}
] |
[
{
"id": "split_0_train_8979_entity",
"type": "progene_text",
"text": [
"BMK1"
],
"offsets": [
[
14,
18
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5816
|
split_0_train_5816
|
[
{
"id": "split_0_train_5816_passage",
"type": "progene_text",
"text": [
"The ability of PMA to partially suppress TRAIL - and TNF - induced cell death was inhibited by BMK1 / DN ."
],
"offsets": [
[
0,
106
]
]
}
] |
[
{
"id": "split_0_train_8980_entity",
"type": "progene_text",
"text": [
"TRAIL"
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"offsets": [
[
41,
46
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],
"normalized": []
},
{
"id": "split_0_train_8981_entity",
"type": "progene_text",
"text": [
"TNF"
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"offsets": [
[
53,
56
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],
"normalized": []
},
{
"id": "split_0_train_8982_entity",
"type": "progene_text",
"text": [
"BMK1"
],
"offsets": [
[
95,
99
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5817
|
split_0_train_5817
|
[
{
"id": "split_0_train_5817_passage",
"type": "progene_text",
"text": [
"However , only TRAIL - induced activity suppression reached statistical significance ( P < .05 ) ."
],
"offsets": [
[
0,
98
]
]
}
] |
[
{
"id": "split_0_train_8983_entity",
"type": "progene_text",
"text": [
"TRAIL"
],
"offsets": [
[
15,
20
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5818
|
split_0_train_5818
|
[
{
"id": "split_0_train_5818_passage",
"type": "progene_text",
"text": [
"CONCLUSIONS :"
],
"offsets": [
[
0,
13
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5819
|
split_0_train_5819
|
[
{
"id": "split_0_train_5819_passage",
"type": "progene_text",
"text": [
"The overexpression of MEK5 in APO - MCF-7 breast carcinoma cells shows that this MAPK signaling protein represents a potent survival molecule ."
],
"offsets": [
[
0,
143
]
]
}
] |
[
{
"id": "split_0_train_8984_entity",
"type": "progene_text",
"text": [
"MEK5"
],
"offsets": [
[
22,
26
]
],
"normalized": []
},
{
"id": "split_0_train_8985_entity",
"type": "progene_text",
"text": [
"MAPK"
],
"offsets": [
[
81,
85
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5820
|
split_0_train_5820
|
[
{
"id": "split_0_train_5820_passage",
"type": "progene_text",
"text": [
"Molecular inhibition of MEK5 signaling may represent a mechanism for sensitizing cancer cells to chemotherapeutic regimens ."
],
"offsets": [
[
0,
124
]
]
}
] |
[
{
"id": "split_0_train_8986_entity",
"type": "progene_text",
"text": [
"MEK5"
],
"offsets": [
[
24,
28
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5821
|
split_0_train_5821
|
[
{
"id": "split_0_train_5821_passage",
"type": "progene_text",
"text": [
"IL-12 plays a significant role in the apoptosis of human T cells in the absence of antigenic stimulation ."
],
"offsets": [
[
0,
106
]
]
}
] |
[
{
"id": "split_0_train_8987_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
0,
5
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5822
|
split_0_train_5822
|
[
{
"id": "split_0_train_5822_passage",
"type": "progene_text",
"text": [
"Interleukin-12 ( IL-12 ) is an immunoregulatory cytokine that plays an essential role in cell - mediated immunity ."
],
"offsets": [
[
0,
115
]
]
}
] |
[
{
"id": "split_0_train_8988_entity",
"type": "progene_text",
"text": [
"Interleukin-12"
],
"offsets": [
[
0,
14
]
],
"normalized": []
},
{
"id": "split_0_train_8989_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
17,
22
]
],
"normalized": []
},
{
"id": "split_0_train_8990_entity",
"type": "progene_text",
"text": [
"cytokine"
],
"offsets": [
[
48,
56
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5823
|
split_0_train_5823
|
[
{
"id": "split_0_train_5823_passage",
"type": "progene_text",
"text": [
"It is known to induce T cell apoptosis in in vivo systems such as graft - versus - host disease ( GVHD ) and experimental autoimmune uveitis ( EAU ) ."
],
"offsets": [
[
0,
150
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5824
|
split_0_train_5824
|
[
{
"id": "split_0_train_5824_passage",
"type": "progene_text",
"text": [
"However , the role of IL-12 in T cell apoptosis in the absence of antigenic stimulation has not been clearly defined ."
],
"offsets": [
[
0,
118
]
]
}
] |
[
{
"id": "split_0_train_8991_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
22,
27
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5825
|
split_0_train_5825
|
[
{
"id": "split_0_train_5825_passage",
"type": "progene_text",
"text": [
"This study was conducted to investigate whether IL-12 , in the absence of an antigen , is able to induce T cell apoptosis , and also , which signalling pathways utilized by IL-12 are involved in this process ."
],
"offsets": [
[
0,
209
]
]
}
] |
[
{
"id": "split_0_train_8992_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
48,
53
]
],
"normalized": []
},
{
"id": "split_0_train_8993_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
173,
178
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5826
|
split_0_train_5826
|
[
{
"id": "split_0_train_5826_passage",
"type": "progene_text",
"text": [
"Our data clearly showed that IL-12 in the absence of an antigen induces apoptosis in T cells ."
],
"offsets": [
[
0,
94
]
]
}
] |
[
{
"id": "split_0_train_8994_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
29,
34
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5827
|
split_0_train_5827
|
[
{
"id": "split_0_train_5827_passage",
"type": "progene_text",
"text": [
"Flow cytometry and ELISA showed FasL up - regulation and increased IFN-gamma synthesis in IL-12 treated T cells , while Fas and TNF-R1 showed little change ."
],
"offsets": [
[
0,
157
]
]
}
] |
[
{
"id": "split_0_train_8995_entity",
"type": "progene_text",
"text": [
"IFN-gamma"
],
"offsets": [
[
67,
76
]
],
"normalized": []
},
{
"id": "split_0_train_8996_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
90,
95
]
],
"normalized": []
},
{
"id": "split_0_train_8997_entity",
"type": "progene_text",
"text": [
"Fas"
],
"offsets": [
[
120,
123
]
],
"normalized": []
},
{
"id": "split_0_train_8998_entity",
"type": "progene_text",
"text": [
"TNF-R1"
],
"offsets": [
[
128,
134
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5828
|
split_0_train_5828
|
[
{
"id": "split_0_train_5828_passage",
"type": "progene_text",
"text": [
"Semi - quantitative RT - PCR demonstrated that IL-12 was able to up - regulate TNF-alpha and FasL mRNA expression ."
],
"offsets": [
[
0,
115
]
]
}
] |
[
{
"id": "split_0_train_8999_entity",
"type": "progene_text",
"text": [
"IL-12"
],
"offsets": [
[
47,
52
]
],
"normalized": []
},
{
"id": "split_0_train_9000_entity",
"type": "progene_text",
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[] |
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split_0_train_5830
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[] |
split_0_train_5831
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split_0_train_5831
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[] |
[] |
split_0_train_5832
|
split_0_train_5832
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[] |
split_0_train_5833
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split_0_train_5833
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[] |
[] |
split_0_train_5834
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split_0_train_5834
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[] |
[] |
split_0_train_5835
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split_0_train_5835
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[] |
[] |
split_0_train_5836
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split_0_train_5836
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[] |
[] |
[] |
split_0_train_5837
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split_0_train_5837
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[] |
[] |
[] |
split_0_train_5838
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split_0_train_5838
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[] |
[] |
[] |
split_0_train_5839
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split_0_train_5839
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[] |
[] |
[] |
split_0_train_5840
|
split_0_train_5840
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[] |
[] |
split_0_train_5841
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split_0_train_5841
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[] |
[] |
split_0_train_5842
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split_0_train_5842
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[] |
[] |
[] |
[] |
split_0_train_5843
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split_0_train_5843
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[] |
[] |
split_0_train_5844
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split_0_train_5844
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[] |
[] |
split_0_train_5845
|
split_0_train_5845
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173
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[] |
[] |
[] |
split_0_train_5846
|
split_0_train_5846
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[] |
[] |
[] |
[] |
split_0_train_5847
|
split_0_train_5847
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[] |
[] |
[] |
split_0_train_5848
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split_0_train_5848
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[] |
[] |
split_0_train_5849
|
split_0_train_5849
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[] |
[] |
[] |
split_0_train_5850
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split_0_train_5850
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28,
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[] |
[] |
split_0_train_5851
|
split_0_train_5851
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[] |
[] |
[] |
split_0_train_5852
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split_0_train_5852
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[] |
[] |
split_0_train_5853
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split_0_train_5853
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[] |
[] |
[] |
split_0_train_5854
|
split_0_train_5854
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[] |
[] |
split_0_train_5855
|
split_0_train_5855
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"AMPA receptor"
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68,
81
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},
{
"id": "split_0_train_9052_entity",
"type": "progene_text",
"text": [
"AMPA receptors"
],
"offsets": [
[
174,
188
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5856
|
split_0_train_5856
|
[
{
"id": "split_0_train_5856_passage",
"type": "progene_text",
"text": [
"[ The role of lipid metabolism in Alzheimer 's disease ]"
],
"offsets": [
[
0,
56
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5857
|
split_0_train_5857
|
[
{
"id": "split_0_train_5857_passage",
"type": "progene_text",
"text": [
"Lipid metabolism in the central nervous system has been focused as an important factor of Alzheimer 's disease , since the apolipoprotein E gene was discovered as a genetic risk for the disease ."
],
"offsets": [
[
0,
195
]
]
}
] |
[
{
"id": "split_0_train_9053_entity",
"type": "progene_text",
"text": [
"apolipoprotein E"
],
"offsets": [
[
123,
139
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5858
|
split_0_train_5858
|
[
{
"id": "split_0_train_5858_passage",
"type": "progene_text",
"text": [
"Lipid metabolism in the brain , showing relatively closed environment , necessitates lipid reutilization ."
],
"offsets": [
[
0,
106
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5859
|
split_0_train_5859
|
[
{
"id": "split_0_train_5859_passage",
"type": "progene_text",
"text": [
"Cerebrospinal fluid contains only high - density lipoproteins composed of apoE and apoJ secreted from astrocytes and of apoA-I and apoA-II transported via the blood brain barrier ."
],
"offsets": [
[
0,
180
]
]
}
] |
[
{
"id": "split_0_train_9054_entity",
"type": "progene_text",
"text": [
"high - density lipoproteins"
],
"offsets": [
[
34,
61
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],
"normalized": []
},
{
"id": "split_0_train_9055_entity",
"type": "progene_text",
"text": [
"apoE"
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"offsets": [
[
74,
78
]
],
"normalized": []
},
{
"id": "split_0_train_9056_entity",
"type": "progene_text",
"text": [
"apoJ"
],
"offsets": [
[
83,
87
]
],
"normalized": []
},
{
"id": "split_0_train_9057_entity",
"type": "progene_text",
"text": [
"apoA-I"
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[
120,
126
]
],
"normalized": []
},
{
"id": "split_0_train_9058_entity",
"type": "progene_text",
"text": [
"apoA-II"
],
"offsets": [
[
131,
138
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5860
|
split_0_train_5860
|
[
{
"id": "split_0_train_5860_passage",
"type": "progene_text",
"text": [
"These apolipoproteins can bind to beta amyloid and possibly relate to its clearance ."
],
"offsets": [
[
0,
85
]
]
}
] |
[
{
"id": "split_0_train_9059_entity",
"type": "progene_text",
"text": [
"apolipoproteins"
],
"offsets": [
[
6,
21
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5861
|
split_0_train_5861
|
[
{
"id": "split_0_train_5861_passage",
"type": "progene_text",
"text": [
"The aggregation of phosphorylated tau , found in neurofibrillary tangles in Alzheimer 's brain , is also found in the brain with Niemann - Pick disease , suggesting that the impairment of lipid transport in neuronal cells participates in Alzheimer 's disease ."
],
"offsets": [
[
0,
260
]
]
}
] |
[
{
"id": "split_0_train_9060_entity",
"type": "progene_text",
"text": [
"tau"
],
"offsets": [
[
34,
37
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5862
|
split_0_train_5862
|
[
{
"id": "split_0_train_5862_passage",
"type": "progene_text",
"text": [
"Mitochondrial function , lipid production , and acetylcholine production are closely related , and these alterations could be involved in cholinergic dysfunction in Alzheimer 's disease ."
],
"offsets": [
[
0,
187
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5863
|
split_0_train_5863
|
[
{
"id": "split_0_train_5863_passage",
"type": "progene_text",
"text": [
"The regulation of lipid metabolism in and outside the brain could be a therapeutic and preventive target for Alzheimer 's disease ."
],
"offsets": [
[
0,
131
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5864
|
split_0_train_5864
|
[
{
"id": "split_0_train_5864_passage",
"type": "progene_text",
"text": [
"Killer Ig - like receptor haplotype analysis by gene content : evidence for genomic diversity with a minimum of six basic framework haplotypes , each with multiple subsets ."
],
"offsets": [
[
0,
173
]
]
}
] |
[
{
"id": "split_0_train_9061_entity",
"type": "progene_text",
"text": [
"Killer Ig - like receptor"
],
"offsets": [
[
0,
25
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5865
|
split_0_train_5865
|
[
{
"id": "split_0_train_5865_passage",
"type": "progene_text",
"text": [
"Killer Ig - like receptor ( KIR ) genes constitute a multigene family whose genomic diversity is achieved through differences in gene content and allelic polymorphism ."
],
"offsets": [
[
0,
168
]
]
}
] |
[
{
"id": "split_0_train_9062_entity",
"type": "progene_text",
"text": [
"Killer Ig - like receptor"
],
"offsets": [
[
0,
25
]
],
"normalized": []
},
{
"id": "split_0_train_9063_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
28,
31
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5866
|
split_0_train_5866
|
[
{
"id": "split_0_train_5866_passage",
"type": "progene_text",
"text": [
"KIR haplotypes containing a single activating KIR gene ( A-haplotypes ) , and KIR haplotypes with multiple activating receptor genes ( B-haplotypes ) have been described ."
],
"offsets": [
[
0,
171
]
]
}
] |
[
{
"id": "split_0_train_9064_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
0,
3
]
],
"normalized": []
},
{
"id": "split_0_train_9065_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
46,
49
]
],
"normalized": []
},
{
"id": "split_0_train_9066_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
78,
81
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5867
|
split_0_train_5867
|
[
{
"id": "split_0_train_5867_passage",
"type": "progene_text",
"text": [
"We report the evaluation of KIR gene content in extended families , sibling pairs , and an unrelated Caucasian panel through identification of the presence or absence of 14 KIR genes and 2 pseudogenes ."
],
"offsets": [
[
0,
202
]
]
}
] |
[
{
"id": "split_0_train_9067_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
28,
31
]
],
"normalized": []
},
{
"id": "split_0_train_9068_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
173,
176
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5868
|
split_0_train_5868
|
[
{
"id": "split_0_train_5868_passage",
"type": "progene_text",
"text": [
"Haplotype definition included subtyping for the expressed and nonexpressed KIR2DL5 variants , for two alleles of pseudogene 3DP1 , and for two alleles of 2DS4 , including a novel 2DS4 allele , KIR1D ."
],
"offsets": [
[
0,
200
]
]
}
] |
[
{
"id": "split_0_train_9069_entity",
"type": "progene_text",
"text": [
"KIR2DL5"
],
"offsets": [
[
75,
82
]
],
"normalized": []
},
{
"id": "split_0_train_9070_entity",
"type": "progene_text",
"text": [
"3DP1"
],
"offsets": [
[
124,
128
]
],
"normalized": []
},
{
"id": "split_0_train_9071_entity",
"type": "progene_text",
"text": [
"2DS4"
],
"offsets": [
[
154,
158
]
],
"normalized": []
},
{
"id": "split_0_train_9072_entity",
"type": "progene_text",
"text": [
"2DS4"
],
"offsets": [
[
179,
183
]
],
"normalized": []
},
{
"id": "split_0_train_9073_entity",
"type": "progene_text",
"text": [
"KIR1D"
],
"offsets": [
[
193,
198
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5869
|
split_0_train_5869
|
[
{
"id": "split_0_train_5869_passage",
"type": "progene_text",
"text": [
"KIR1D appears functionally homologous to the rhesus monkey KIR1D and likely arose as a consequence of a 22 nucleotide deletion in the coding sequence of 2DS4 , leading to disruption of Ig - domain 2D and a premature termination codon following the first amino acid in the putative transmembrane domain ."
],
"offsets": [
[
0,
303
]
]
}
] |
[
{
"id": "split_0_train_9074_entity",
"type": "progene_text",
"text": [
"KIR1D"
],
"offsets": [
[
0,
5
]
],
"normalized": []
},
{
"id": "split_0_train_9075_entity",
"type": "progene_text",
"text": [
"KIR1D"
],
"offsets": [
[
59,
64
]
],
"normalized": []
},
{
"id": "split_0_train_9076_entity",
"type": "progene_text",
"text": [
"2DS4"
],
"offsets": [
[
153,
157
]
],
"normalized": []
},
{
"id": "split_0_train_9077_entity",
"type": "progene_text",
"text": [
"Ig"
],
"offsets": [
[
185,
187
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5870
|
split_0_train_5870
|
[
{
"id": "split_0_train_5870_passage",
"type": "progene_text",
"text": [
"Our investigations identified 11 haplotypes within 12 families ."
],
"offsets": [
[
0,
64
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5871
|
split_0_train_5871
|
[
{
"id": "split_0_train_5871_passage",
"type": "progene_text",
"text": [
"From 49 sibling pairs and 17 consanguineous DNA samples , an additional 12 haplotypes were predicted ."
],
"offsets": [
[
0,
102
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5872
|
split_0_train_5872
|
[
{
"id": "split_0_train_5872_passage",
"type": "progene_text",
"text": [
"Our studies support a model for KIR haplotype diversity based on six basic gene compositions ."
],
"offsets": [
[
0,
94
]
]
}
] |
[
{
"id": "split_0_train_9078_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
32,
35
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5873
|
split_0_train_5873
|
[
{
"id": "split_0_train_5873_passage",
"type": "progene_text",
"text": [
"We suggest that the centromeric half of the KIR genomic region is comprised of three major combinations , while the telomeric half can assume a short form with either 2DS4 or KIR1D or a long form with multiple combinations of several stimulatory KIR genes ."
],
"offsets": [
[
0,
257
]
]
}
] |
[
{
"id": "split_0_train_9079_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
44,
47
]
],
"normalized": []
},
{
"id": "split_0_train_9080_entity",
"type": "progene_text",
"text": [
"2DS4"
],
"offsets": [
[
167,
171
]
],
"normalized": []
},
{
"id": "split_0_train_9081_entity",
"type": "progene_text",
"text": [
"KIR1D"
],
"offsets": [
[
175,
180
]
],
"normalized": []
},
{
"id": "split_0_train_9082_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
246,
249
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5874
|
split_0_train_5874
|
[
{
"id": "split_0_train_5874_passage",
"type": "progene_text",
"text": [
"Additional rare haplotypes can be identified , and may have arisen by gene duplication , intergenic recombination , or deletions ."
],
"offsets": [
[
0,
130
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5875
|
split_0_train_5875
|
[
{
"id": "split_0_train_5875_passage",
"type": "progene_text",
"text": [
"Identification of a specific molecular repressor of the peroxisome proliferator - activated receptor gamma Coactivator-1 alpha ( PGC-1alpha ) ."
],
"offsets": [
[
0,
143
]
]
}
] |
[
{
"id": "split_0_train_9083_entity",
"type": "progene_text",
"text": [
"peroxisome proliferator - activated receptor gamma Coactivator-1 alpha"
],
"offsets": [
[
56,
126
]
],
"normalized": []
},
{
"id": "split_0_train_9084_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
129,
139
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5876
|
split_0_train_5876
|
[
{
"id": "split_0_train_5876_passage",
"type": "progene_text",
"text": [
"The nuclear co - activator PGC-1alpha is a pivotal regulator of numerous pathways controlling both metabolism and overall energy homeostasis ."
],
"offsets": [
[
0,
142
]
]
}
] |
[
{
"id": "split_0_train_9085_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
27,
37
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5877
|
split_0_train_5877
|
[
{
"id": "split_0_train_5877_passage",
"type": "progene_text",
"text": [
"Inappropriate increases in PGC-1alpha activity have been linked to a number of pathological conditions including heart failure and diabetes mellitus ."
],
"offsets": [
[
0,
150
]
]
}
] |
[
{
"id": "split_0_train_9086_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
27,
37
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5878
|
split_0_train_5878
|
[
{
"id": "split_0_train_5878_passage",
"type": "progene_text",
"text": [
"Previous studies ( Puigserver , P. , Adelmant , G. , Wu , Z. , Fan , M. , Xu , J. , O ' Malley , B. , and Spiegelman , B. M. ( 1999 ) Science 286 , 1368 - 1371 ) have demonstrated an inhibitory domain within PGC-1alpha that limits transcriptional activity ."
],
"offsets": [
[
0,
257
]
]
}
] |
[
{
"id": "split_0_train_9087_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
208,
218
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5879
|
split_0_train_5879
|
[
{
"id": "split_0_train_5879_passage",
"type": "progene_text",
"text": [
"Using this inhibitory domain in a yeast two - hybrid screen , we demonstrate that PGC-1alpha directly associates with the orphan nuclear receptor estrogen - related receptor - alpha ( ERR-alpha ) ."
],
"offsets": [
[
0,
197
]
]
}
] |
[
{
"id": "split_0_train_9088_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
82,
92
]
],
"normalized": []
},
{
"id": "split_0_train_9089_entity",
"type": "progene_text",
"text": [
"estrogen - related receptor - alpha"
],
"offsets": [
[
146,
181
]
],
"normalized": []
},
{
"id": "split_0_train_9090_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
184,
193
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5880
|
split_0_train_5880
|
[
{
"id": "split_0_train_5880_passage",
"type": "progene_text",
"text": [
"The binding of ERR-alpha to PGC-1alpha requires the C - terminal AF2 domain of ERR-alpha ."
],
"offsets": [
[
0,
90
]
]
}
] |
[
{
"id": "split_0_train_9091_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
15,
24
]
],
"normalized": []
},
{
"id": "split_0_train_9092_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
28,
38
]
],
"normalized": []
},
{
"id": "split_0_train_9093_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
79,
88
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5881
|
split_0_train_5881
|
[
{
"id": "split_0_train_5881_passage",
"type": "progene_text",
"text": [
"PGC-1alpha and ERR-alpha have a similar pattern of expression in human tissues , with both being present predominantly in organs with high metabolic needs such as skeletal muscle and kidney ."
],
"offsets": [
[
0,
191
]
]
}
] |
[
{
"id": "split_0_train_9094_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
0,
10
]
],
"normalized": []
},
{
"id": "split_0_train_9095_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
15,
24
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5882
|
split_0_train_5882
|
[
{
"id": "split_0_train_5882_passage",
"type": "progene_text",
"text": [
"Similarly , we show that in mice physiological stimuli such as fasting coordinately induces PGC-1alpha and ERR-alpha transcription ."
],
"offsets": [
[
0,
132
]
]
}
] |
[
{
"id": "split_0_train_9096_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
92,
102
]
],
"normalized": []
},
{
"id": "split_0_train_9097_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
107,
116
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5883
|
split_0_train_5883
|
[
{
"id": "split_0_train_5883_passage",
"type": "progene_text",
"text": [
"We also demonstrate that under normal conditions PGC-1alpha is located within discrete nuclear speckles , whereas the expression of ERR-alpha results in PGC-1alpha redistributing uniformly throughout the nucleoplasm ."
],
"offsets": [
[
0,
217
]
]
}
] |
[
{
"id": "split_0_train_9098_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
49,
59
]
],
"normalized": []
},
{
"id": "split_0_train_9099_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
132,
141
]
],
"normalized": []
},
{
"id": "split_0_train_9100_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
153,
163
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5884
|
split_0_train_5884
|
[
{
"id": "split_0_train_5884_passage",
"type": "progene_text",
"text": [
"Finally , we show that the expression of ERR-alpha can dramatically and specifically repress PGC-1alpha transcriptional activity ."
],
"offsets": [
[
0,
130
]
]
}
] |
[
{
"id": "split_0_train_9101_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
41,
50
]
],
"normalized": []
},
{
"id": "split_0_train_9102_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
93,
103
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5885
|
split_0_train_5885
|
[
{
"id": "split_0_train_5885_passage",
"type": "progene_text",
"text": [
"These results suggest a novel mechanism of transcriptional control wherein ERR-alpha can function as a specific molecular repressor of PGC-1alpha activity ."
],
"offsets": [
[
0,
156
]
]
}
] |
[
{
"id": "split_0_train_9103_entity",
"type": "progene_text",
"text": [
"ERR-alpha"
],
"offsets": [
[
75,
84
]
],
"normalized": []
},
{
"id": "split_0_train_9104_entity",
"type": "progene_text",
"text": [
"PGC-1alpha"
],
"offsets": [
[
135,
145
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5886
|
split_0_train_5886
|
[
{
"id": "split_0_train_5886_passage",
"type": "progene_text",
"text": [
"In addition , our results suggest that other co - activators might also have specific repressors , thereby identifying another layer of combinatorial complexity in transcriptional regulation ."
],
"offsets": [
[
0,
192
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5887
|
split_0_train_5887
|
[
{
"id": "split_0_train_5887_passage",
"type": "progene_text",
"text": [
"The expression of alpha-dystrobrevin and dystrophin during skeletal muscle regeneration ."
],
"offsets": [
[
0,
89
]
]
}
] |
[
{
"id": "split_0_train_9105_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
18,
36
]
],
"normalized": []
},
{
"id": "split_0_train_9106_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
41,
51
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5888
|
split_0_train_5888
|
[
{
"id": "split_0_train_5888_passage",
"type": "progene_text",
"text": [
"The expression of alpha-dystrobrevin and dystrophin in rat tibialis anterior muscles was chronologically evaluated during a cycle of regeneration after myonecrosis induced by the injection of cardiotoxin ."
],
"offsets": [
[
0,
205
]
]
}
] |
[
{
"id": "split_0_train_9107_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
18,
36
]
],
"normalized": []
},
{
"id": "split_0_train_9108_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
41,
51
]
],
"normalized": []
},
{
"id": "split_0_train_9109_entity",
"type": "progene_text",
"text": [
"cardiotoxin"
],
"offsets": [
[
192,
203
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5889
|
split_0_train_5889
|
[
{
"id": "split_0_train_5889_passage",
"type": "progene_text",
"text": [
"In immunohistochemical studies , alpha-dystrobrevin and dystrophin were first stained weakly at the sarcolemma of some regenerating muscle fibers on day 5 ."
],
"offsets": [
[
0,
156
]
]
}
] |
[
{
"id": "split_0_train_9110_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
33,
51
]
],
"normalized": []
},
{
"id": "split_0_train_9111_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
56,
66
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5890
|
split_0_train_5890
|
[
{
"id": "split_0_train_5890_passage",
"type": "progene_text",
"text": [
"On day 7 , alpha-dystrobrevin was still stained weakly , whereas dystrophin was stained conspicuously ."
],
"offsets": [
[
0,
103
]
]
}
] |
[
{
"id": "split_0_train_9112_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
11,
29
]
],
"normalized": []
},
{
"id": "split_0_train_9113_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
65,
75
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5891
|
split_0_train_5891
|
[
{
"id": "split_0_train_5891_passage",
"type": "progene_text",
"text": [
"After day 10 , alpha - dystrobrevin and dystrophin were both stained conspicuously on almost all regenerating muscle fibers ."
],
"offsets": [
[
0,
125
]
]
}
] |
[
{
"id": "split_0_train_9114_entity",
"type": "progene_text",
"text": [
"alpha - dystrobrevin"
],
"offsets": [
[
15,
35
]
],
"normalized": []
},
{
"id": "split_0_train_9115_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
40,
50
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5892
|
split_0_train_5892
|
[
{
"id": "split_0_train_5892_passage",
"type": "progene_text",
"text": [
"In the Western blot analysis , alpha-dystrobrevin and dystrophin were first detected as visible bands on days 5 and 7 , respectively ."
],
"offsets": [
[
0,
134
]
]
}
] |
[
{
"id": "split_0_train_9116_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
31,
49
]
],
"normalized": []
},
{
"id": "split_0_train_9117_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
54,
64
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5893
|
split_0_train_5893
|
[
{
"id": "split_0_train_5893_passage",
"type": "progene_text",
"text": [
"The bands of alpha-dystrobrevin and dystrophin both darkened sequentially up to day 10 ."
],
"offsets": [
[
0,
88
]
]
}
] |
[
{
"id": "split_0_train_9118_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
13,
31
]
],
"normalized": []
},
{
"id": "split_0_train_9119_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
36,
46
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5894
|
split_0_train_5894
|
[
{
"id": "split_0_train_5894_passage",
"type": "progene_text",
"text": [
"The protein levels based on the densitometrical analysis of the bands on each day were converted to the percentage of the protein level on day 28 , which was taken as 100 % ."
],
"offsets": [
[
0,
174
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5895
|
split_0_train_5895
|
[
{
"id": "split_0_train_5895_passage",
"type": "progene_text",
"text": [
"The sequential line based on these data showed that alpha-dystrobrevin and dystrophin reached 50 % of the protein level on day 28 by 6.6 and 5.3 days , respectively ."
],
"offsets": [
[
0,
166
]
]
}
] |
[
{
"id": "split_0_train_9120_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
52,
70
]
],
"normalized": []
},
{
"id": "split_0_train_9121_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
75,
85
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5896
|
split_0_train_5896
|
[
{
"id": "split_0_train_5896_passage",
"type": "progene_text",
"text": [
"These data provide evidence that alpha-dystrobrevin regenerates more slowly than dystrophin in skeletal muscle ."
],
"offsets": [
[
0,
112
]
]
}
] |
[
{
"id": "split_0_train_9122_entity",
"type": "progene_text",
"text": [
"alpha-dystrobrevin"
],
"offsets": [
[
33,
51
]
],
"normalized": []
},
{
"id": "split_0_train_9123_entity",
"type": "progene_text",
"text": [
"dystrophin"
],
"offsets": [
[
81,
91
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5897
|
split_0_train_5897
|
[
{
"id": "split_0_train_5897_passage",
"type": "progene_text",
"text": [
"Expression of hpttg proto - oncogene in lymphoid neoplasias ."
],
"offsets": [
[
0,
61
]
]
}
] |
[
{
"id": "split_0_train_9124_entity",
"type": "progene_text",
"text": [
"hpttg"
],
"offsets": [
[
14,
19
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5898
|
split_0_train_5898
|
[
{
"id": "split_0_train_5898_passage",
"type": "progene_text",
"text": [
"Pituitary tumor - transforming gene ( pttg ) is a distinct proto - oncogene which is expressed in certain normal tissues with high proliferation rate and in a variety of tumors ."
],
"offsets": [
[
0,
178
]
]
}
] |
[
{
"id": "split_0_train_9125_entity",
"type": "progene_text",
"text": [
"Pituitary tumor - transforming gene"
],
"offsets": [
[
0,
35
]
],
"normalized": []
},
{
"id": "split_0_train_9126_entity",
"type": "progene_text",
"text": [
"pttg"
],
"offsets": [
[
38,
42
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5899
|
split_0_train_5899
|
[
{
"id": "split_0_train_5899_passage",
"type": "progene_text",
"text": [
"PTTG is the vertebrate analog of yeast securins Pds1 and Cut2 with a key role in the regulation of sister chromatid separation during mitosis ."
],
"offsets": [
[
0,
143
]
]
}
] |
[
{
"id": "split_0_train_9127_entity",
"type": "progene_text",
"text": [
"PTTG"
],
"offsets": [
[
0,
4
]
],
"normalized": []
},
{
"id": "split_0_train_9128_entity",
"type": "progene_text",
"text": [
"securins"
],
"offsets": [
[
39,
47
]
],
"normalized": []
},
{
"id": "split_0_train_9129_entity",
"type": "progene_text",
"text": [
"Pds1"
],
"offsets": [
[
48,
52
]
],
"normalized": []
},
{
"id": "split_0_train_9130_entity",
"type": "progene_text",
"text": [
"Cut2"
],
"offsets": [
[
57,
61
]
],
"normalized": []
}
] |
[] |
[] |
[] |
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