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stringlengths 15
19
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stringlengths 15
19
| passages
list | entities
list | events
list | coreferences
list | relations
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|---|---|---|---|---|---|---|
split_0_train_5100
|
split_0_train_5100
|
[
{
"id": "split_0_train_5100_passage",
"type": "progene_text",
"text": [
"Only one case showed pathological HFA results , while FOP was normal ."
],
"offsets": [
[
0,
70
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5101
|
split_0_train_5101
|
[
{
"id": "split_0_train_5101_passage",
"type": "progene_text",
"text": [
"Detection rates of VFDs significantly differed between the two methods ( p < 0.001 ; sign test ) ."
],
"offsets": [
[
0,
98
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5102
|
split_0_train_5102
|
[
{
"id": "split_0_train_5102_passage",
"type": "progene_text",
"text": [
"CONCLUSIONS :"
],
"offsets": [
[
0,
13
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5103
|
split_0_train_5103
|
[
{
"id": "split_0_train_5103_passage",
"type": "progene_text",
"text": [
"FOP , using individually condensed test grids , significantly increases detection rates of glaucomatous VFDs in morphologically suspicuous areas compared with a conventional HFA 30 - 2 technique using equidistant rectangular ( 6 degrees x 6 degrees ) test point arrangements ."
],
"offsets": [
[
0,
276
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]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5104
|
split_0_train_5104
|
[
{
"id": "split_0_train_5104_passage",
"type": "progene_text",
"text": [
"Single - stranded nucleic acid - binding protein , Pur alpha , interacts with RNA homologous to 18S ribosomal RNA and inhibits translation in vitro ."
],
"offsets": [
[
0,
149
]
]
}
] |
[
{
"id": "split_0_train_8165_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
51,
60
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5105
|
split_0_train_5105
|
[
{
"id": "split_0_train_5105_passage",
"type": "progene_text",
"text": [
"Pur alpha is a highly conserved , eukaryotic sequence - specific DNA - and RNA - binding protein involved in diverse cellular and viral functions including transcription , replication , and cell growth ."
],
"offsets": [
[
0,
203
]
]
}
] |
[
{
"id": "split_0_train_8166_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
0,
9
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5106
|
split_0_train_5106
|
[
{
"id": "split_0_train_5106_passage",
"type": "progene_text",
"text": [
"Pur alpha exerts its activity in part by interacting with other viral and cellular proteins ."
],
"offsets": [
[
0,
93
]
]
}
] |
[
{
"id": "split_0_train_8167_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
0,
9
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5107
|
split_0_train_5107
|
[
{
"id": "split_0_train_5107_passage",
"type": "progene_text",
"text": [
"One such protein is the human immunodeficiency virus ( HIV ) type I regulatory protein Tat ."
],
"offsets": [
[
0,
92
]
]
}
] |
[
{
"id": "split_0_train_8168_entity",
"type": "progene_text",
"text": [
"Tat"
],
"offsets": [
[
87,
90
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5108
|
split_0_train_5108
|
[
{
"id": "split_0_train_5108_passage",
"type": "progene_text",
"text": [
"Earlier studies have demonstrated that this interaction is mediated by Pur alpha - associated RNA ( PARNA ) and that RNA immunopurified from mammalian expressed Pur alpha was capable of reconstituting the interaction between these two proteins ."
],
"offsets": [
[
0,
245
]
]
}
] |
[
{
"id": "split_0_train_8169_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
71,
80
]
],
"normalized": []
},
{
"id": "split_0_train_8170_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
161,
170
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5109
|
split_0_train_5109
|
[
{
"id": "split_0_train_5109_passage",
"type": "progene_text",
"text": [
"In the current study , we characterize four RNA species which were immunopurified with Pur alpha ."
],
"offsets": [
[
0,
98
]
]
}
] |
[
{
"id": "split_0_train_8171_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
87,
96
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5110
|
split_0_train_5110
|
[
{
"id": "split_0_train_5110_passage",
"type": "progene_text",
"text": [
"Northern blot analysis with one of the PARNAs revealed a highly abundant signal of approximately 2.0 kilobases ( kb ) present in all cell lines tested ."
],
"offsets": [
[
0,
152
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5111
|
split_0_train_5111
|
[
{
"id": "split_0_train_5111_passage",
"type": "progene_text",
"text": [
"Sequence analysis of each of the four PARNA clones revealed a high homology to different regions of the human 18S ribosomal RNA sequence ."
],
"offsets": [
[
0,
138
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5112
|
split_0_train_5112
|
[
{
"id": "split_0_train_5112_passage",
"type": "progene_text",
"text": [
"Based on this homology , we investigated the influence of Pur alpha on translation ."
],
"offsets": [
[
0,
84
]
]
}
] |
[
{
"id": "split_0_train_8172_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
58,
67
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5113
|
split_0_train_5113
|
[
{
"id": "split_0_train_5113_passage",
"type": "progene_text",
"text": [
"Luciferase assays were performed after coupled in vitro transcription / translation reactions with a vector containing a luciferase reporter construct and increasing concentrations of BSA , GST , and GST - Pur alpha ."
],
"offsets": [
[
0,
217
]
]
}
] |
[
{
"id": "split_0_train_8173_entity",
"type": "progene_text",
"text": [
"Luciferase"
],
"offsets": [
[
0,
10
]
],
"normalized": []
},
{
"id": "split_0_train_8174_entity",
"type": "progene_text",
"text": [
"luciferase"
],
"offsets": [
[
121,
131
]
],
"normalized": []
},
{
"id": "split_0_train_8175_entity",
"type": "progene_text",
"text": [
"BSA"
],
"offsets": [
[
184,
187
]
],
"normalized": []
},
{
"id": "split_0_train_8176_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
190,
193
]
],
"normalized": []
},
{
"id": "split_0_train_8177_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
200,
203
]
],
"normalized": []
},
{
"id": "split_0_train_8178_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
206,
215
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5114
|
split_0_train_5114
|
[
{
"id": "split_0_train_5114_passage",
"type": "progene_text",
"text": [
"Inclusion of GST - Pur alpha in these reactions resulted in a dose - dependent inhibition of luciferase activity ."
],
"offsets": [
[
0,
114
]
]
}
] |
[
{
"id": "split_0_train_8179_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
13,
16
]
],
"normalized": []
},
{
"id": "split_0_train_8180_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
19,
28
]
],
"normalized": []
},
{
"id": "split_0_train_8181_entity",
"type": "progene_text",
"text": [
"luciferase"
],
"offsets": [
[
93,
103
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5115
|
split_0_train_5115
|
[
{
"id": "split_0_train_5115_passage",
"type": "progene_text",
"text": [
"Similar inhibition was observed with in vitro translation reactions performed with in vitro transcribed luciferase RNA and increasing concentrations of GST - Pur alpha ."
],
"offsets": [
[
0,
169
]
]
}
] |
[
{
"id": "split_0_train_8182_entity",
"type": "progene_text",
"text": [
"luciferase"
],
"offsets": [
[
104,
114
]
],
"normalized": []
},
{
"id": "split_0_train_8183_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
152,
155
]
],
"normalized": []
},
{
"id": "split_0_train_8184_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
158,
167
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5116
|
split_0_train_5116
|
[
{
"id": "split_0_train_5116_passage",
"type": "progene_text",
"text": [
"In control experiments , inclusion of increasing concentrations of GST - Pur alpha with luciferase protein resulted in no effect on luciferase activity ."
],
"offsets": [
[
0,
153
]
]
}
] |
[
{
"id": "split_0_train_8185_entity",
"type": "progene_text",
"text": [
"GST"
],
"offsets": [
[
67,
70
]
],
"normalized": []
},
{
"id": "split_0_train_8186_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
73,
82
]
],
"normalized": []
},
{
"id": "split_0_train_8187_entity",
"type": "progene_text",
"text": [
"luciferase"
],
"offsets": [
[
88,
98
]
],
"normalized": []
},
{
"id": "split_0_train_8188_entity",
"type": "progene_text",
"text": [
"luciferase"
],
"offsets": [
[
132,
142
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5117
|
split_0_train_5117
|
[
{
"id": "split_0_train_5117_passage",
"type": "progene_text",
"text": [
"Taken together , these data demonstrate that Pur alpha inhibits translation reactions in vitro ."
],
"offsets": [
[
0,
96
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5118
|
split_0_train_5118
|
[
{
"id": "split_0_train_5118_passage",
"type": "progene_text",
"text": [
"Moreover , this Pur alpha - mediated inhibition of translation can be abrogated by HIV-1 Tat protein ."
],
"offsets": [
[
0,
102
]
]
}
] |
[
{
"id": "split_0_train_8189_entity",
"type": "progene_text",
"text": [
"Pur alpha"
],
"offsets": [
[
16,
25
]
],
"normalized": []
},
{
"id": "split_0_train_8190_entity",
"type": "progene_text",
"text": [
"Tat"
],
"offsets": [
[
89,
92
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5119
|
split_0_train_5119
|
[
{
"id": "split_0_train_5119_passage",
"type": "progene_text",
"text": [
"Comparison of spinal cord gray matter and white matter softness : measurement by pipette aspiration method ."
],
"offsets": [
[
0,
108
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5120
|
split_0_train_5120
|
[
{
"id": "split_0_train_5120_passage",
"type": "progene_text",
"text": [
"OBJECT :"
],
"offsets": [
[
0,
8
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5121
|
split_0_train_5121
|
[
{
"id": "split_0_train_5121_passage",
"type": "progene_text",
"text": [
"Although the gray matter of the spinal cord has been thought to be softer than the white matter , there is no evidence to support this belief ."
],
"offsets": [
[
0,
143
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5122
|
split_0_train_5122
|
[
{
"id": "split_0_train_5122_passage",
"type": "progene_text",
"text": [
"Because the spinal cord is extremely soft , it has been difficult to measure the mechanical properties of the gray and white matter ."
],
"offsets": [
[
0,
133
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5123
|
split_0_train_5123
|
[
{
"id": "split_0_train_5123_passage",
"type": "progene_text",
"text": [
"The modulis of elasticity of the gray and white matter were measured in situ by using a pipette aspiration method ."
],
"offsets": [
[
0,
115
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5124
|
split_0_train_5124
|
[
{
"id": "split_0_train_5124_passage",
"type": "progene_text",
"text": [
"METHOD :"
],
"offsets": [
[
0,
8
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5125
|
split_0_train_5125
|
[
{
"id": "split_0_train_5125_passage",
"type": "progene_text",
"text": [
"The spinal cord specimens were excised from Japanese white rabbits ."
],
"offsets": [
[
0,
68
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5126
|
split_0_train_5126
|
[
{
"id": "split_0_train_5126_passage",
"type": "progene_text",
"text": [
"Specimens were cut to display the surfaces of axial , frontal , and sagittal sections ."
],
"offsets": [
[
0,
87
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5127
|
split_0_train_5127
|
[
{
"id": "split_0_train_5127_passage",
"type": "progene_text",
"text": [
"The surfaces of the gray and white matter were aspirated using a 0.8 -mm-inner-diameter glass pipette while monitoring with a video microscope , and the deformed length in the pipette was measured on a monitor ."
],
"offsets": [
[
0,
211
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5128
|
split_0_train_5128
|
[
{
"id": "split_0_train_5128_passage",
"type": "progene_text",
"text": [
"In each case the modulus of elasticity was calculated by comparing the relationship between the aspiration pressure and aspirated volume of the specimen with that determined by finite element analysis ."
],
"offsets": [
[
0,
202
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5129
|
split_0_train_5129
|
[
{
"id": "split_0_train_5129_passage",
"type": "progene_text",
"text": [
"The moduli of elasticity of the gray and white matter were 3.4 +/- 1.4 kPa ( mean +/- standard deviation ) and 3.4 +/- 0.9 kPa in the axial section , 3+/- 0.3 kPa and 3.5 +/- 0.5 kPa in the frontal section , and 3.5 +/- 0.9 kPa and 2.8 +/- 0.4 kPa in the sagittal section , respectively ."
],
"offsets": [
[
0,
288
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5130
|
split_0_train_5130
|
[
{
"id": "split_0_train_5130_passage",
"type": "progene_text",
"text": [
"CONCLUSIONS :"
],
"offsets": [
[
0,
13
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5131
|
split_0_train_5131
|
[
{
"id": "split_0_train_5131_passage",
"type": "progene_text",
"text": [
"No significant difference in modulus of elasticity was shown between the gray and white matter of the spinal in sections made in various directions ."
],
"offsets": [
[
0,
149
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5132
|
split_0_train_5132
|
[
{
"id": "split_0_train_5132_passage",
"type": "progene_text",
"text": [
"Sequence analysis of a fish vitellogenin cDNA with a large phosvitin domain ."
],
"offsets": [
[
0,
77
]
]
}
] |
[
{
"id": "split_0_train_8191_entity",
"type": "progene_text",
"text": [
"vitellogenin"
],
"offsets": [
[
28,
40
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],
"normalized": []
},
{
"id": "split_0_train_8192_entity",
"type": "progene_text",
"text": [
"phosvitin"
],
"offsets": [
[
59,
68
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5133
|
split_0_train_5133
|
[
{
"id": "split_0_train_5133_passage",
"type": "progene_text",
"text": [
"Vitellogenins ( Vtg ) are egg - yolk precursor proteins crucial for reproductive success in oviparous animals ."
],
"offsets": [
[
0,
111
]
]
}
] |
[
{
"id": "split_0_train_8193_entity",
"type": "progene_text",
"text": [
"Vitellogenins"
],
"offsets": [
[
0,
13
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5134
|
split_0_train_5134
|
[
{
"id": "split_0_train_5134_passage",
"type": "progene_text",
"text": [
"We have cloned the first complete cichlid Vtg cDNA from the tilapia fish , Oreochromis aureus ."
],
"offsets": [
[
0,
95
]
]
}
] |
[
{
"id": "split_0_train_8194_entity",
"type": "progene_text",
"text": [
"Vtg"
],
"offsets": [
[
42,
45
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5135
|
split_0_train_5135
|
[
{
"id": "split_0_train_5135_passage",
"type": "progene_text",
"text": [
"This cDNA has the largest phosvitin ( PV ) domain amongst piscine Vtgs , being comparable to those of lamprey , Xenopus , and chicken ."
],
"offsets": [
[
0,
135
]
]
}
] |
[
{
"id": "split_0_train_8195_entity",
"type": "progene_text",
"text": [
"phosvitin"
],
"offsets": [
[
26,
35
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],
"normalized": []
},
{
"id": "split_0_train_8196_entity",
"type": "progene_text",
"text": [
"PV"
],
"offsets": [
[
38,
40
]
],
"normalized": []
},
{
"id": "split_0_train_8197_entity",
"type": "progene_text",
"text": [
"Vtgs"
],
"offsets": [
[
66,
70
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5136
|
split_0_train_5136
|
[
{
"id": "split_0_train_5136_passage",
"type": "progene_text",
"text": [
"Thus , the size of PV is independent of the evolutionary advancement of a species ."
],
"offsets": [
[
0,
83
]
]
}
] |
[
{
"id": "split_0_train_8198_entity",
"type": "progene_text",
"text": [
"PV"
],
"offsets": [
[
19,
21
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5137
|
split_0_train_5137
|
[
{
"id": "split_0_train_5137_passage",
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"The closer interspecific relationship between O. aureus Vtg1 and Fundulus VtgII than the intraspecific relationship between Fundulus VtgI and II isoforms suggests that teleost ancestors had at least two Vtg isoforms ."
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"Vtg"
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203,
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] |
[] |
[] |
[] |
split_0_train_5138
|
split_0_train_5138
|
[
{
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"type": "progene_text",
"text": [
"Contrary to the results of previous phylogenetic inference using Vtgs which indicate that insect lineage is most diverged and nematodes are closer to vertebrate lineage , our results show that nematodes and hexapods form two monophyletic sister groups ."
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[
0,
253
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[
{
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"type": "progene_text",
"text": [
"Vtgs"
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[
65,
69
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}
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[] |
[] |
[] |
split_0_train_5139
|
split_0_train_5139
|
[
{
"id": "split_0_train_5139_passage",
"type": "progene_text",
"text": [
"Another arthropod taxon , represented by a malacostracan crustacean , Penaeus japonicus , appears to be more closely related to the vertebrates than the hexapods ."
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[
0,
163
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]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5140
|
split_0_train_5140
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[
{
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"type": "progene_text",
"text": [
"Periodontal inflammation and insulin resistance -- lessons from obesity ."
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"offsets": [
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0,
73
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{
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"type": "progene_text",
"text": [
"insulin"
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[
29,
36
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}
] |
[] |
[] |
[] |
split_0_train_5141
|
split_0_train_5141
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[
{
"id": "split_0_train_5141_passage",
"type": "progene_text",
"text": [
"Recent attention has been focused on our understanding of the negative influences of oral chronic inflammation on systemic health ."
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"offsets": [
[
0,
131
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]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5142
|
split_0_train_5142
|
[
{
"id": "split_0_train_5142_passage",
"type": "progene_text",
"text": [
"Successful periodontal treatment appears to have beneficial effects on the metabolic control of type 2 diabetes ."
],
"offsets": [
[
0,
113
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]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5143
|
split_0_train_5143
|
[
{
"id": "split_0_train_5143_passage",
"type": "progene_text",
"text": [
"Although type 2 diabetes is a multiple - risk - factor syndrome , lowered insulin sensitivity , called insulin resistance , is essential in developing the disease ."
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[
0,
164
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}
] |
[
{
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{
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"type": "progene_text",
"text": [
"insulin"
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"offsets": [
[
103,
110
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}
] |
[] |
[] |
[] |
split_0_train_5144
|
split_0_train_5144
|
[
{
"id": "split_0_train_5144_passage",
"type": "progene_text",
"text": [
"Pro - inflammatory cytokine , tumor necrosis factor - alpha ( TNF-alpha ) , produced from adipose tissues in obese subjects , is known to play a predominant role in inducing insulin resistance ."
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[
0,
194
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]
}
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[
{
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{
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{
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62,
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{
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"type": "progene_text",
"text": [
"insulin"
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"offsets": [
[
174,
181
]
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"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5145
|
split_0_train_5145
|
[
{
"id": "split_0_train_5145_passage",
"type": "progene_text",
"text": [
"Therefore , it can be hypothesized that anti - infectious periodontal treatment may improve metabolic control of diabetes via improved insulin sensitivity by reducing peripheral TNF-alpha concentration ."
],
"offsets": [
[
0,
203
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]
}
] |
[
{
"id": "split_0_train_8211_entity",
"type": "progene_text",
"text": [
"insulin"
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135,
142
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{
"id": "split_0_train_8212_entity",
"type": "progene_text",
"text": [
"TNF-alpha"
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"offsets": [
[
178,
187
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"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5146
|
split_0_train_5146
|
[
{
"id": "split_0_train_5146_passage",
"type": "progene_text",
"text": [
"In this review , we summarize the nature of insulin resistance and discuss the mechanisms by which insulin sensitivity is influenced by chronic inflammation , such as in periodontal disease ."
],
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[
0,
191
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]
}
] |
[
{
"id": "split_0_train_8213_entity",
"type": "progene_text",
"text": [
"insulin"
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44,
51
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{
"id": "split_0_train_8214_entity",
"type": "progene_text",
"text": [
"insulin"
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"offsets": [
[
99,
106
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5147
|
split_0_train_5147
|
[
{
"id": "split_0_train_5147_passage",
"type": "progene_text",
"text": [
"Effect of diabetes on nitric oxide metabolism during cardiac surgery ."
],
"offsets": [
[
0,
70
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5148
|
split_0_train_5148
|
[
{
"id": "split_0_train_5148_passage",
"type": "progene_text",
"text": [
"The metabolism of nitric oxide ( NO ) during cardiac surgery is unclear ."
],
"offsets": [
[
0,
73
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5149
|
split_0_train_5149
|
[
{
"id": "split_0_train_5149_passage",
"type": "progene_text",
"text": [
"We studied the effect of diabetes on NO metabolism during cardiac surgery in 40 subjects ( 20 with diabetes and 20 without diabetes ) ."
],
"offsets": [
[
0,
135
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5150
|
split_0_train_5150
|
[
{
"id": "split_0_train_5150_passage",
"type": "progene_text",
"text": [
"The patients were randomized to receive an infusion of physiological saline or nitroglycerin ( GTN ) at 1 microg. kg(-1) ."
],
"offsets": [
[
0,
122
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5151
|
split_0_train_5151
|
[
{
"id": "split_0_train_5151_passage",
"type": "progene_text",
"text": [
"min(-1) starting 10 min before the initiation of cardiopulmonary bypass and then continuing for a period of 4 h ."
],
"offsets": [
[
0,
113
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5152
|
split_0_train_5152
|
[
{
"id": "split_0_train_5152_passage",
"type": "progene_text",
"text": [
"Blood and urine samples were collected at several time points for up to 8 h ."
],
"offsets": [
[
0,
77
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5153
|
split_0_train_5153
|
[
{
"id": "split_0_train_5153_passage",
"type": "progene_text",
"text": [
"NO metabolites were determined by the measurement of nitrate / nitrite ( NOx , micromol / mmol creatinine ) and cyclic guanosine monophosphate ( cGMP , nmol / mmol creatinine ) in plasma and urine ."
],
"offsets": [
[
0,
198
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5154
|
split_0_train_5154
|
[
{
"id": "split_0_train_5154_passage",
"type": "progene_text",
"text": [
"Plasma insulin levels were also determined at selected time points ."
],
"offsets": [
[
0,
68
]
]
}
] |
[
{
"id": "split_0_train_8215_entity",
"type": "progene_text",
"text": [
"insulin"
],
"offsets": [
[
7,
14
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5155
|
split_0_train_5155
|
[
{
"id": "split_0_train_5155_passage",
"type": "progene_text",
"text": [
"Plasma NOx levels before surgery were significantly elevated in the group with diabetes compared with the group without diabetes ( P < 0.001 ) , and values were further increased during surgery in the former ( P = 0.005 ) but not in the latter ( P = 0.8 ) ."
],
"offsets": [
[
0,
257
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5156
|
split_0_train_5156
|
[
{
"id": "split_0_train_5156_passage",
"type": "progene_text",
"text": [
"The greater plasma NOx values in patients with diabetes were matched by commensurate elevations in plasma cGMP levels ( P = 0.01 ) ."
],
"offsets": [
[
0,
132
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5157
|
split_0_train_5157
|
[
{
"id": "split_0_train_5157_passage",
"type": "progene_text",
"text": [
"Interestingly , infusion of GTN , an NO donor , significantly reduced plasma NOx ( P < 0.001 ) and its urine elimination ( P < 0.001 ) in patients with diabetes without reducing plasma cGMP levels ( P = 0.89 ) ."
],
"offsets": [
[
0,
211
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5158
|
split_0_train_5158
|
[
{
"id": "split_0_train_5158_passage",
"type": "progene_text",
"text": [
"Cardiac surgery increased plasma insulin in patients with and without diabetes ; this increase was delayed by the infusion of GTN , but it was not related to the changes in NO production ."
],
"offsets": [
[
0,
188
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5159
|
split_0_train_5159
|
[
{
"id": "split_0_train_5159_passage",
"type": "progene_text",
"text": [
"In conclusion , NO production during cardiac surgery is increased in patients with diabetes , and this elevation can be blunted by the infusion of GTN in a rapid and reversible manner ."
],
"offsets": [
[
0,
185
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5160
|
split_0_train_5160
|
[
{
"id": "split_0_train_5160_passage",
"type": "progene_text",
"text": [
"Control elements of Dictyostelium discoideum prespore specific gene 3B ."
],
"offsets": [
[
0,
72
]
]
}
] |
[
{
"id": "split_0_train_8216_entity",
"type": "progene_text",
"text": [
"prespore specific gene 3B"
],
"offsets": [
[
45,
70
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5161
|
split_0_train_5161
|
[
{
"id": "split_0_train_5161_passage",
"type": "progene_text",
"text": [
"Expression of the prespore - specific gene 3B in Dictyostelium discoideum Ax-2 cells is first detectable late in development with 3B mRNA levels peaking at 18 h ( Corney et al. , 1990 ) ."
],
"offsets": [
[
0,
187
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]
}
] |
[
{
"id": "split_0_train_8217_entity",
"type": "progene_text",
"text": [
"prespore - specific gene 3B"
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"offsets": [
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18,
45
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{
"id": "split_0_train_8218_entity",
"type": "progene_text",
"text": [
"3B"
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"offsets": [
[
130,
132
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5162
|
split_0_train_5162
|
[
{
"id": "split_0_train_5162_passage",
"type": "progene_text",
"text": [
"Sequence analysis of 3B cDNA and genomic clones revealed two exons , 319bp and 341bp long , separated by an 82bp intron , which encode a 219 residue protein with no significant similarity to any other reported gene product ."
],
"offsets": [
[
0,
224
]
]
}
] |
[
{
"id": "split_0_train_8219_entity",
"type": "progene_text",
"text": [
"3B"
],
"offsets": [
[
21,
23
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5163
|
split_0_train_5163
|
[
{
"id": "split_0_train_5163_passage",
"type": "progene_text",
"text": [
"Transcription starts at an A residue 45bp upstream from the translation initiation codon , preceded by a TATA - like sequence and an oligo - dT stretch ."
],
"offsets": [
[
0,
153
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5164
|
split_0_train_5164
|
[
{
"id": "split_0_train_5164_passage",
"type": "progene_text",
"text": [
"The 5' flanking sequence of the 3B gene is extremely A + T rich but contains five G / C rich stretches , each approximately 7bp long , which have strong sequence similarity to the G boxes found upstream of other developmentally regulated Dictyostelium genes ."
],
"offsets": [
[
0,
259
]
]
}
] |
[
{
"id": "split_0_train_8220_entity",
"type": "progene_text",
"text": [
"3B"
],
"offsets": [
[
32,
34
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5165
|
split_0_train_5165
|
[
{
"id": "split_0_train_5165_passage",
"type": "progene_text",
"text": [
"Analysis of both 3B promoter - CAT reporter gene and 3B promoter - lacZ reporter gene constructs showed that 908bp of 5' flanking sequence is sufficient to confer correct developmental and cell - type specific regulation ."
],
"offsets": [
[
0,
222
]
]
}
] |
[
{
"id": "split_0_train_8221_entity",
"type": "progene_text",
"text": [
"3B"
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"offsets": [
[
17,
19
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"normalized": []
},
{
"id": "split_0_train_8222_entity",
"type": "progene_text",
"text": [
"CAT"
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"offsets": [
[
31,
34
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"normalized": []
},
{
"id": "split_0_train_8223_entity",
"type": "progene_text",
"text": [
"3B"
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"offsets": [
[
53,
55
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"normalized": []
},
{
"id": "split_0_train_8224_entity",
"type": "progene_text",
"text": [
"lacZ"
],
"offsets": [
[
67,
71
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5166
|
split_0_train_5166
|
[
{
"id": "split_0_train_5166_passage",
"type": "progene_text",
"text": [
"Sequential 5' deletion analysis revealed that positive elements lie upstream of position - 304 and that negative element(s) lie between positions - 264 and - 241 ."
],
"offsets": [
[
0,
163
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5167
|
split_0_train_5167
|
[
{
"id": "split_0_train_5167_passage",
"type": "progene_text",
"text": [
"Nevertheless , a 286bp promoter fragment containing only sequence located downstream of position - 241 directed essentially correct reporter gene expression ."
],
"offsets": [
[
0,
158
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5168
|
split_0_train_5168
|
[
{
"id": "split_0_train_5168_passage",
"type": "progene_text",
"text": [
"Point mutation analysis identified cis - acting elements within this ' sufficient ' promoter fragment which activate transcription ( G box V and psp - AT type sequences ) ."
],
"offsets": [
[
0,
172
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5169
|
split_0_train_5169
|
[
{
"id": "split_0_train_5169_passage",
"type": "progene_text",
"text": [
"A short ( 56bp ) region of the 3B promoter sequence containing both G box IV and the psp - AT type element binds two types of nuclear factor , one present in cells throughout development and a second that appears only in late development with a time course comparable to 3B gene induction ."
],
"offsets": [
[
0,
290
]
]
}
] |
[
{
"id": "split_0_train_8225_entity",
"type": "progene_text",
"text": [
"3B"
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"offsets": [
[
31,
33
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],
"normalized": []
},
{
"id": "split_0_train_8226_entity",
"type": "progene_text",
"text": [
"3B"
],
"offsets": [
[
271,
273
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5170
|
split_0_train_5170
|
[
{
"id": "split_0_train_5170_passage",
"type": "progene_text",
"text": [
"Leukocyte receptor complex - encoded immunomodulatory receptors show differing specificity for alternative HLA-B27 structures ."
],
"offsets": [
[
0,
127
]
]
}
] |
[
{
"id": "split_0_train_8227_entity",
"type": "progene_text",
"text": [
"HLA-B27"
],
"offsets": [
[
107,
114
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5171
|
split_0_train_5171
|
[
{
"id": "split_0_train_5171_passage",
"type": "progene_text",
"text": [
"We studied recognition of the disease - associated HLA-B27 allele by immunomodulatory receptors encoded within the leukocyte receptor complex ."
],
"offsets": [
[
0,
143
]
]
}
] |
[
{
"id": "split_0_train_8228_entity",
"type": "progene_text",
"text": [
"HLA-B27"
],
"offsets": [
[
51,
58
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5172
|
split_0_train_5172
|
[
{
"id": "split_0_train_5172_passage",
"type": "progene_text",
"text": [
"HLA class I are ligands for members of the killer Ig receptor ( KIR ) and Ig - like transcript ( ILT ) / LIR / LILR families ( the new LILR nomenclature is described at www. gene.ucl.ac.uk / nomenclature / genefamily / lilr . html ) ."
],
"offsets": [
[
0,
234
]
]
}
] |
[
{
"id": "split_0_train_8229_entity",
"type": "progene_text",
"text": [
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[
0,
11
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"normalized": []
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{
"id": "split_0_train_8230_entity",
"type": "progene_text",
"text": [
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43,
61
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"normalized": []
},
{
"id": "split_0_train_8231_entity",
"type": "progene_text",
"text": [
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"offsets": [
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64,
67
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"normalized": []
},
{
"id": "split_0_train_8232_entity",
"type": "progene_text",
"text": [
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"offsets": [
[
74,
94
]
],
"normalized": []
},
{
"id": "split_0_train_8233_entity",
"type": "progene_text",
"text": [
"ILT"
],
"offsets": [
[
97,
100
]
],
"normalized": []
},
{
"id": "split_0_train_8234_entity",
"type": "progene_text",
"text": [
"LIR"
],
"offsets": [
[
105,
108
]
],
"normalized": []
},
{
"id": "split_0_train_8235_entity",
"type": "progene_text",
"text": [
"LILR"
],
"offsets": [
[
111,
115
]
],
"normalized": []
},
{
"id": "split_0_train_8236_entity",
"type": "progene_text",
"text": [
"LILR"
],
"offsets": [
[
135,
139
]
],
"normalized": []
},
{
"id": "split_0_train_8237_entity",
"type": "progene_text",
"text": [
"lilr"
],
"offsets": [
[
219,
223
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5173
|
split_0_train_5173
|
[
{
"id": "split_0_train_5173_passage",
"type": "progene_text",
"text": [
"Members of these families bound HLA-B27 in both classical and beta(2) microglobulin - independent forms ."
],
"offsets": [
[
0,
105
]
]
}
] |
[
{
"id": "split_0_train_8238_entity",
"type": "progene_text",
"text": [
"HLA-B27"
],
"offsets": [
[
32,
39
]
],
"normalized": []
},
{
"id": "split_0_train_8239_entity",
"type": "progene_text",
"text": [
"beta(2) microglobulin"
],
"offsets": [
[
62,
83
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5174
|
split_0_train_5174
|
[
{
"id": "split_0_train_5174_passage",
"type": "progene_text",
"text": [
"Classical complexes bound ILT2 , ILT4 , and LIR6 transfectants but not ILT1 , ILT3 , or ILT5 ."
],
"offsets": [
[
0,
94
]
]
}
] |
[
{
"id": "split_0_train_8240_entity",
"type": "progene_text",
"text": [
"ILT2"
],
"offsets": [
[
26,
30
]
],
"normalized": []
},
{
"id": "split_0_train_8241_entity",
"type": "progene_text",
"text": [
"ILT4"
],
"offsets": [
[
33,
37
]
],
"normalized": []
},
{
"id": "split_0_train_8242_entity",
"type": "progene_text",
"text": [
"LIR6"
],
"offsets": [
[
44,
48
]
],
"normalized": []
},
{
"id": "split_0_train_8243_entity",
"type": "progene_text",
"text": [
"ILT1"
],
"offsets": [
[
71,
75
]
],
"normalized": []
},
{
"id": "split_0_train_8244_entity",
"type": "progene_text",
"text": [
"ILT3"
],
"offsets": [
[
78,
82
]
],
"normalized": []
},
{
"id": "split_0_train_8245_entity",
"type": "progene_text",
"text": [
"ILT5"
],
"offsets": [
[
88,
92
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5175
|
split_0_train_5175
|
[
{
"id": "split_0_train_5175_passage",
"type": "progene_text",
"text": [
"A free H chain form of HLA-B27 bound ILT4 and LIR6 ."
],
"offsets": [
[
0,
52
]
]
}
] |
[
{
"id": "split_0_train_8246_entity",
"type": "progene_text",
"text": [
"HLA-B27"
],
"offsets": [
[
23,
30
]
],
"normalized": []
},
{
"id": "split_0_train_8247_entity",
"type": "progene_text",
"text": [
"ILT4"
],
"offsets": [
[
37,
41
]
],
"normalized": []
},
{
"id": "split_0_train_8248_entity",
"type": "progene_text",
"text": [
"LIR6"
],
"offsets": [
[
46,
50
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5176
|
split_0_train_5176
|
[
{
"id": "split_0_train_5176_passage",
"type": "progene_text",
"text": [
"Both forms of HLA-B27 bound KIR3DL1 transfectants ."
],
"offsets": [
[
0,
51
]
]
}
] |
[
{
"id": "split_0_train_8249_entity",
"type": "progene_text",
"text": [
"HLA-B27"
],
"offsets": [
[
14,
21
]
],
"normalized": []
},
{
"id": "split_0_train_8250_entity",
"type": "progene_text",
"text": [
"KIR3DL1"
],
"offsets": [
[
28,
35
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5177
|
split_0_train_5177
|
[
{
"id": "split_0_train_5177_passage",
"type": "progene_text",
"text": [
"HLA-B27 free H chain bound CD14 ( + ) cells in PBL from healthy controls , consistent with ILT4 expression on monocytes ."
],
"offsets": [
[
0,
121
]
]
}
] |
[
{
"id": "split_0_train_8251_entity",
"type": "progene_text",
"text": [
"HLA-B27"
],
"offsets": [
[
0,
7
]
],
"normalized": []
},
{
"id": "split_0_train_8252_entity",
"type": "progene_text",
"text": [
"CD14"
],
"offsets": [
[
27,
31
]
],
"normalized": []
},
{
"id": "split_0_train_8253_entity",
"type": "progene_text",
"text": [
"ILT4"
],
"offsets": [
[
91,
95
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5178
|
split_0_train_5178
|
[
{
"id": "split_0_train_5178_passage",
"type": "progene_text",
"text": [
"Alternative recognition of different forms of HLA-B27 by KIR or ILT could influence their immunomodulatory function and may imply a role in inflammatory disease ."
],
"offsets": [
[
0,
162
]
]
}
] |
[
{
"id": "split_0_train_8254_entity",
"type": "progene_text",
"text": [
"HLA-B27"
],
"offsets": [
[
46,
53
]
],
"normalized": []
},
{
"id": "split_0_train_8255_entity",
"type": "progene_text",
"text": [
"KIR"
],
"offsets": [
[
57,
60
]
],
"normalized": []
},
{
"id": "split_0_train_8256_entity",
"type": "progene_text",
"text": [
"ILT"
],
"offsets": [
[
64,
67
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5179
|
split_0_train_5179
|
[
{
"id": "split_0_train_5179_passage",
"type": "progene_text",
"text": [
"Growth hormone and insulin - like growth factor I receptors in the temporomandibular joint of the rat ."
],
"offsets": [
[
0,
103
]
]
}
] |
[
{
"id": "split_0_train_8257_entity",
"type": "progene_text",
"text": [
"Growth hormone and insulin - like growth factor I receptors"
],
"offsets": [
[
0,
59
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5180
|
split_0_train_5180
|
[
{
"id": "split_0_train_5180_passage",
"type": "progene_text",
"text": [
"While there are numerous investigations on hormonal control of long bone epiphyseal growth , corresponding knowledge is sparse concerning the condylar cartilage ."
],
"offsets": [
[
0,
162
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5181
|
split_0_train_5181
|
[
{
"id": "split_0_train_5181_passage",
"type": "progene_text",
"text": [
"We investigated the distribution of growth hormone ( GH ) and insulin - like growth factor I ( IGF-I ) receptors in the temporomandibular joint ( TMJ ) , especially the condyle , and compared the findings with information of long bone epiphyseal plates ."
],
"offsets": [
[
0,
254
]
]
}
] |
[
{
"id": "split_0_train_8258_entity",
"type": "progene_text",
"text": [
"growth hormone ( GH ) and insulin - like growth factor I ( IGF-I ) receptors"
],
"offsets": [
[
36,
112
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5182
|
split_0_train_5182
|
[
{
"id": "split_0_train_5182_passage",
"type": "progene_text",
"text": [
"The localization of the receptors was examined in vivo by immunohistochemical methods in one - to 21 - day - old rats ."
],
"offsets": [
[
0,
119
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5183
|
split_0_train_5183
|
[
{
"id": "split_0_train_5183_passage",
"type": "progene_text",
"text": [
"GH receptors were detected in various components of the TMJ , but not in the fibrous articular surface or in the cartilage layers of the condyle ."
],
"offsets": [
[
0,
146
]
]
}
] |
[
{
"id": "split_0_train_8259_entity",
"type": "progene_text",
"text": [
"GH receptors"
],
"offsets": [
[
0,
12
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5184
|
split_0_train_5184
|
[
{
"id": "split_0_train_5184_passage",
"type": "progene_text",
"text": [
"IGF-I receptors were found in the fibrous articular surface of the condyle and particularly in the superior and posterosuperior regions of the condylar cartilage , the depth of the labeled cell layer increasing significantly with age ."
],
"offsets": [
[
0,
235
]
]
}
] |
[
{
"id": "split_0_train_8260_entity",
"type": "progene_text",
"text": [
"IGF-I receptors"
],
"offsets": [
[
0,
15
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5185
|
split_0_train_5185
|
[
{
"id": "split_0_train_5185_passage",
"type": "progene_text",
"text": [
"It is evident that the expression of GH and IGF-I receptors is area - specific in the TMJ ."
],
"offsets": [
[
0,
91
]
]
}
] |
[
{
"id": "split_0_train_8261_entity",
"type": "progene_text",
"text": [
"GH and IGF-I receptors"
],
"offsets": [
[
37,
59
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5186
|
split_0_train_5186
|
[
{
"id": "split_0_train_5186_passage",
"type": "progene_text",
"text": [
"Early post - natal growth and development of the mandibular condylar cartilage seem to be IGF-I - dependent but not directly dependent on GH ."
],
"offsets": [
[
0,
142
]
]
}
] |
[
{
"id": "split_0_train_8262_entity",
"type": "progene_text",
"text": [
"IGF-I"
],
"offsets": [
[
90,
95
]
],
"normalized": []
},
{
"id": "split_0_train_8263_entity",
"type": "progene_text",
"text": [
"GH"
],
"offsets": [
[
138,
140
]
],
"normalized": []
}
] |
[] |
[] |
[] |
split_0_train_5187
|
split_0_train_5187
|
[
{
"id": "split_0_train_5187_passage",
"type": "progene_text",
"text": [
"Optimal pinhole techniques for preoperative localization with Tc-99m MIBI for primary hyperparathyroidism ."
],
"offsets": [
[
0,
107
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5188
|
split_0_train_5188
|
[
{
"id": "split_0_train_5188_passage",
"type": "progene_text",
"text": [
"PURPOSE :"
],
"offsets": [
[
0,
9
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5189
|
split_0_train_5189
|
[
{
"id": "split_0_train_5189_passage",
"type": "progene_text",
"text": [
"Technetium-99m-labeled 2-methoxyisobutylisonitrile ( Tc-99m MIBI ) has been used extensively to localize parathyroid adenomas before operation ."
],
"offsets": [
[
0,
144
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5190
|
split_0_train_5190
|
[
{
"id": "split_0_train_5190_passage",
"type": "progene_text",
"text": [
"Imaging techniques vary widely , and the aim of this study was to determine the optimal time of delayed imaging and the value of routine correlative pertechnetate thyroid imaging ."
],
"offsets": [
[
0,
180
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5191
|
split_0_train_5191
|
[
{
"id": "split_0_train_5191_passage",
"type": "progene_text",
"text": [
"MATERIALS AND METHODS :"
],
"offsets": [
[
0,
23
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5192
|
split_0_train_5192
|
[
{
"id": "split_0_train_5192_passage",
"type": "progene_text",
"text": [
"In this study , preoperative parathyroid localization was performed using pinhole anterior and oblique images ( 15 minutes and 2 and 4 hours after injection ) with correlative pertechnetate thyroid images ."
],
"offsets": [
[
0,
206
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5193
|
split_0_train_5193
|
[
{
"id": "split_0_train_5193_passage",
"type": "progene_text",
"text": [
"Ninety - seven patients underwent dual - or triple - phase Tc-99m MIBI imaging and correlative pertechnetate thyroid imaging before surgery ."
],
"offsets": [
[
0,
141
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5194
|
split_0_train_5194
|
[
{
"id": "split_0_train_5194_passage",
"type": "progene_text",
"text": [
"Two nuclear medicine physicians blinded to the surgical findings interpreted all available images and various Tc-99m MIBI image combinations at 15 minutes alone ; 15 minutes and 2 hours , 15 minutes and 4 hours ; and 15 minutes and 2 and 4 hours each with and without correlative pertechnetate thyroid imaging ."
],
"offsets": [
[
0,
311
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5195
|
split_0_train_5195
|
[
{
"id": "split_0_train_5195_passage",
"type": "progene_text",
"text": [
"RESULTS :"
],
"offsets": [
[
0,
9
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5196
|
split_0_train_5196
|
[
{
"id": "split_0_train_5196_passage",
"type": "progene_text",
"text": [
"Ninety parathyroid adenomas were detected in 86 patients ."
],
"offsets": [
[
0,
58
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5197
|
split_0_train_5197
|
[
{
"id": "split_0_train_5197_passage",
"type": "progene_text",
"text": [
"The optimal results were achieved with 15 - minute and 2 - and 4 - hour Tc-99m-MIBI images , with correlative thyroid scans resulting in a sensitivity rate of 88 % ."
],
"offsets": [
[
0,
165
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5198
|
split_0_train_5198
|
[
{
"id": "split_0_train_5198_passage",
"type": "progene_text",
"text": [
"Fifteen - minute and 2-hour Tc-99m-MIBI images and correlative thyroid scans and 15 - minute and 4-hour Tc-99m MIBI images and correlative thyroid scans produced similar results ( sensitivity rate , 86 % and 83 % , respectively ; P = not significant ) ."
],
"offsets": [
[
0,
253
]
]
}
] |
[] |
[] |
[] |
[] |
split_0_train_5199
|
split_0_train_5199
|
[
{
"id": "split_0_train_5199_passage",
"type": "progene_text",
"text": [
"Compared with all Tc-99m MIBI image combinations alone , the addition of the routine correlative thyroid scan significantly improved sensitivity and also improved reporter confidence in 45 % of studies ."
],
"offsets": [
[
0,
203
]
]
}
] |
[] |
[] |
[] |
[] |
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