id
stringlengths 15
19
| document_id
stringlengths 15
19
| passages
list | entities
list | events
list | coreferences
list | relations
list |
|---|---|---|---|---|---|---|
split_0_train_1000 | split_0_train_1000 | [
{
"id": "split_0_train_1000_passage",
"type": "progene_text",
"text": [
"None of the anti - beta subunit antibodies reacted with protein extracts of E. coli host cells , suggesting that these bacteria have no beta subunit protein ."
],
"offsets": [
[
0,
158
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1001 | split_0_train_1001 | [
{
"id": "split_0_train_1001_passage",
"type": "progene_text",
"text": [
"Interestingly , the rbeta subunit associated with E. coli as well as human MAT alpha subunits ."
],
"offsets": [
[
0,
95
]
]
}
]
| [
{
"id": "split_0_train_1374_entity",
"type": "progene_text",
"text": [
"MAT alpha"
],
"offsets": [
[
75,
84
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1002 | split_0_train_1002 | [
{
"id": "split_0_train_1002_passage",
"type": "progene_text",
"text": [
"This association changed the kinetic properties of both enzymes and lowered the K(m) of MAT for L-methionine ."
],
"offsets": [
[
0,
110
]
]
}
]
| [
{
"id": "split_0_train_1375_entity",
"type": "progene_text",
"text": [
"MAT"
],
"offsets": [
[
88,
91
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1003 | split_0_train_1003 | [
{
"id": "split_0_train_1003_passage",
"type": "progene_text",
"text": [
"Together , the data show that we have cloned and expressed the human MAT II beta subunit and confirmed its long suspected regulatory function ."
],
"offsets": [
[
0,
143
]
]
}
]
| [
{
"id": "split_0_train_1376_entity",
"type": "progene_text",
"text": [
"MAT II beta"
],
"offsets": [
[
69,
80
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1004 | split_0_train_1004 | [
{
"id": "split_0_train_1004_passage",
"type": "progene_text",
"text": [
"This knowledge affords a molecular means by which MAT activity and consequently the levels of AdoMet may be modulated in mammalian cells ."
],
"offsets": [
[
0,
138
]
]
}
]
| [
{
"id": "split_0_train_1377_entity",
"type": "progene_text",
"text": [
"MAT"
],
"offsets": [
[
50,
53
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1005 | split_0_train_1005 | [
{
"id": "split_0_train_1005_passage",
"type": "progene_text",
"text": [
"Palindromes as substrates for multiple pathways of recombination in Escherichia coli ."
],
"offsets": [
[
0,
86
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1006 | split_0_train_1006 | [
{
"id": "split_0_train_1006_passage",
"type": "progene_text",
"text": [
"A 246 - bp imperfect palindrome has the potential to form hairpin structures in single - stranded DNA during replication ."
],
"offsets": [
[
0,
122
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1007 | split_0_train_1007 | [
{
"id": "split_0_train_1007_passage",
"type": "progene_text",
"text": [
"Genetic evidence suggests that these structures are converted to double - strand breaks by the SbcCD nuclease and that the double - strand breaks are repaired by recombination ."
],
"offsets": [
[
0,
177
]
]
}
]
| [
{
"id": "split_0_train_1378_entity",
"type": "progene_text",
"text": [
"SbcCD nuclease"
],
"offsets": [
[
95,
109
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1008 | split_0_train_1008 | [
{
"id": "split_0_train_1008_passage",
"type": "progene_text",
"text": [
"We investigated the role of a range of recombination mutations on the viability of cells containing this palindrome ."
],
"offsets": [
[
0,
117
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1009 | split_0_train_1009 | [
{
"id": "split_0_train_1009_passage",
"type": "progene_text",
"text": [
"The palindrome was introduced into the Escherichia coli chromosome by phage lambda lysogenization ."
],
"offsets": [
[
0,
99
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1010 | split_0_train_1010 | [
{
"id": "split_0_train_1010_passage",
"type": "progene_text",
"text": [
"This was done in both wt and sbcC backgrounds ."
],
"offsets": [
[
0,
47
]
]
}
]
| [
{
"id": "split_0_train_1379_entity",
"type": "progene_text",
"text": [
"sbcC"
],
"offsets": [
[
29,
33
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1011 | split_0_train_1011 | [
{
"id": "split_0_train_1011_passage",
"type": "progene_text",
"text": [
"Repair of the SbcCD - induced double - strand breaks requires a large number of proteins , including the components of both the RecB and RecF pathways ."
],
"offsets": [
[
0,
152
]
]
}
]
| [
{
"id": "split_0_train_1380_entity",
"type": "progene_text",
"text": [
"SbcCD"
],
"offsets": [
[
14,
19
]
],
"normalized": []
},
{
"id": "split_0_train_1381_entity",
"type": "progene_text",
"text": [
"RecB"
],
"offsets": [
[
128,
132
]
],
"normalized": []
},
{
"id": "split_0_train_1382_entity",
"type": "progene_text",
"text": [
"RecF"
],
"offsets": [
[
137,
141
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1012 | split_0_train_1012 | [
{
"id": "split_0_train_1012_passage",
"type": "progene_text",
"text": [
"Repair does not involve PriA - dependent replication fork restart , which suggests that the double - strand break occurs after the replication fork has passed the palindrome ."
],
"offsets": [
[
0,
175
]
]
}
]
| [
{
"id": "split_0_train_1383_entity",
"type": "progene_text",
"text": [
"PriA"
],
"offsets": [
[
24,
28
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1013 | split_0_train_1013 | [
{
"id": "split_0_train_1013_passage",
"type": "progene_text",
"text": [
"In the absence of SbcCD , recombination still occurs , probably using a gap substrate ."
],
"offsets": [
[
0,
87
]
]
}
]
| [
{
"id": "split_0_train_1384_entity",
"type": "progene_text",
"text": [
"SbcCD"
],
"offsets": [
[
18,
23
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1014 | split_0_train_1014 | [
{
"id": "split_0_train_1014_passage",
"type": "progene_text",
"text": [
"This process is also PriA independent , suggesting that there is no collapse of the replication fork ."
],
"offsets": [
[
0,
102
]
]
}
]
| [
{
"id": "split_0_train_1385_entity",
"type": "progene_text",
"text": [
"PriA"
],
"offsets": [
[
21,
25
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1015 | split_0_train_1015 | [
{
"id": "split_0_train_1015_passage",
"type": "progene_text",
"text": [
"In the absence of RecA , the RecQ helicase is required for palindrome viability in a sbcC mutant , suggesting that a helicase - dependent pathway exists to allow replicative bypass of secondary structures ."
],
"offsets": [
[
0,
206
]
]
}
]
| [
{
"id": "split_0_train_1386_entity",
"type": "progene_text",
"text": [
"RecA"
],
"offsets": [
[
18,
22
]
],
"normalized": []
},
{
"id": "split_0_train_1387_entity",
"type": "progene_text",
"text": [
"RecQ"
],
"offsets": [
[
29,
33
]
],
"normalized": []
},
{
"id": "split_0_train_1388_entity",
"type": "progene_text",
"text": [
"helicase"
],
"offsets": [
[
34,
42
]
],
"normalized": []
},
{
"id": "split_0_train_1389_entity",
"type": "progene_text",
"text": [
"sbcC"
],
"offsets": [
[
85,
89
]
],
"normalized": []
},
{
"id": "split_0_train_1390_entity",
"type": "progene_text",
"text": [
"helicase"
],
"offsets": [
[
117,
125
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1016 | split_0_train_1016 | [
{
"id": "split_0_train_1016_passage",
"type": "progene_text",
"text": [
"Flt3 ligand ( FL ) and its influence on immune reactivity ."
],
"offsets": [
[
0,
59
]
]
}
]
| [
{
"id": "split_0_train_1391_entity",
"type": "progene_text",
"text": [
"Flt3 ligand"
],
"offsets": [
[
0,
11
]
],
"normalized": []
},
{
"id": "split_0_train_1392_entity",
"type": "progene_text",
"text": [
"FL"
],
"offsets": [
[
14,
16
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1017 | split_0_train_1017 | [
{
"id": "split_0_train_1017_passage",
"type": "progene_text",
"text": [
"Flt3 ( fms - like tyrosine kinase 3 ) ligand ( FL ) is a potent hematopoietic cytokine that affects the growth and differentiation of progenitor and stem cells both in vivo and in vitro ."
],
"offsets": [
[
0,
187
]
]
}
]
| [
{
"id": "split_0_train_1393_entity",
"type": "progene_text",
"text": [
"Flt3 ( fms - like tyrosine kinase 3 ) ligand"
],
"offsets": [
[
0,
44
]
],
"normalized": []
},
{
"id": "split_0_train_1394_entity",
"type": "progene_text",
"text": [
"FL"
],
"offsets": [
[
47,
49
]
],
"normalized": []
},
{
"id": "split_0_train_1395_entity",
"type": "progene_text",
"text": [
"cytokine"
],
"offsets": [
[
78,
86
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1018 | split_0_train_1018 | [
{
"id": "split_0_train_1018_passage",
"type": "progene_text",
"text": [
"Its capacity to augment strikingly the numbers of dendritic cells ( rare antigen - presenting cells that induce and regulate immune responses ) in mice and humans has stimulated considerable interest in its value as an investigational tool and therapeutic agent ."
],
"offsets": [
[
0,
263
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1019 | split_0_train_1019 | [
{
"id": "split_0_train_1019_passage",
"type": "progene_text",
"text": [
"In this review , we survey the hematopoietic properties and immunobiology of FL , and examine its therapeutic potential ."
],
"offsets": [
[
0,
121
]
]
}
]
| [
{
"id": "split_0_train_1396_entity",
"type": "progene_text",
"text": [
"FL"
],
"offsets": [
[
77,
79
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1020 | split_0_train_1020 | [
{
"id": "split_0_train_1020_passage",
"type": "progene_text",
"text": [
"Distribution of PDE4A and G(o) alpha immunoreactivity in the accessory olfactory system of the mouse ."
],
"offsets": [
[
0,
102
]
]
}
]
| [
{
"id": "split_0_train_1397_entity",
"type": "progene_text",
"text": [
"PDE4A"
],
"offsets": [
[
16,
21
]
],
"normalized": []
},
{
"id": "split_0_train_1398_entity",
"type": "progene_text",
"text": [
"G(o) alpha"
],
"offsets": [
[
26,
36
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1021 | split_0_train_1021 | [
{
"id": "split_0_train_1021_passage",
"type": "progene_text",
"text": [
"Distribution of the cAMP - specific phosphodiesterase PDE4A was examined in the accessory olfactory system by immunohistochemistry ."
],
"offsets": [
[
0,
132
]
]
}
]
| [
{
"id": "split_0_train_1399_entity",
"type": "progene_text",
"text": [
"phosphodiesterase"
],
"offsets": [
[
36,
53
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],
"normalized": []
},
{
"id": "split_0_train_1400_entity",
"type": "progene_text",
"text": [
"PDE4A"
],
"offsets": [
[
54,
59
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1022 | split_0_train_1022 | [
{
"id": "split_0_train_1022_passage",
"type": "progene_text",
"text": [
"Adjacent sections through the vomeronasal organ ( VNO ) and accessory olfactory bulb ( AOB ) were alternately immunostained with antibodies against PDE4A or the G - protein alpha subunit G ( o ) alpha , which labels basal VNO neurons , in order to determine whether PDE4A occurs preferentially in one of two segregated VNO pathways ."
],
"offsets": [
[
0,
333
]
]
}
]
| [
{
"id": "split_0_train_1401_entity",
"type": "progene_text",
"text": [
"PDE4A"
],
"offsets": [
[
148,
153
]
],
"normalized": []
},
{
"id": "split_0_train_1402_entity",
"type": "progene_text",
"text": [
"G - protein alpha"
],
"offsets": [
[
161,
178
]
],
"normalized": []
},
{
"id": "split_0_train_1403_entity",
"type": "progene_text",
"text": [
"G ( o ) alpha"
],
"offsets": [
[
187,
200
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],
"normalized": []
},
{
"id": "split_0_train_1404_entity",
"type": "progene_text",
"text": [
"PDE4A"
],
"offsets": [
[
266,
271
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1023 | split_0_train_1023 | [
{
"id": "split_0_train_1023_passage",
"type": "progene_text",
"text": [
"We found that PDE4A strongly labeled apical VNO neurons and rostral AOB glomeruli ."
],
"offsets": [
[
0,
83
]
]
}
]
| [
{
"id": "split_0_train_1405_entity",
"type": "progene_text",
"text": [
"PDE4A"
],
"offsets": [
[
14,
19
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1024 | split_0_train_1024 | [
{
"id": "split_0_train_1024_passage",
"type": "progene_text",
"text": [
"There was virtually no overlap in G(o) alpha and PDE4A staining , and there were no regions of the VNO neuroepithelium or AOB glomeruli not labeled by either antibody ."
],
"offsets": [
[
0,
168
]
]
}
]
| [
{
"id": "split_0_train_1406_entity",
"type": "progene_text",
"text": [
"G(o) alpha"
],
"offsets": [
[
34,
44
]
],
"normalized": []
},
{
"id": "split_0_train_1407_entity",
"type": "progene_text",
"text": [
"PDE4A"
],
"offsets": [
[
49,
54
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1025 | split_0_train_1025 | [
{
"id": "split_0_train_1025_passage",
"type": "progene_text",
"text": [
"These results identify a potential member of the pheromone transduction cascade in apical neurons , and provide further evidence that the VNO consists of functionally distinct pathways ."
],
"offsets": [
[
0,
186
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1026 | split_0_train_1026 | [
{
"id": "split_0_train_1026_passage",
"type": "progene_text",
"text": [
"Interactions among components of the Salmonella flagellar export apparatus and its substrates ."
],
"offsets": [
[
0,
95
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1027 | split_0_train_1027 | [
{
"id": "split_0_train_1027_passage",
"type": "progene_text",
"text": [
"We have examined the cytoplasmic components ( FliH , FliI and FliJ ) of the type III flagellar protein export apparatus , plus the cytoplasmic domains ( FlhAC and FlhBC ) of two of its six membrane components ."
],
"offsets": [
[
0,
210
]
]
}
]
| [
{
"id": "split_0_train_1408_entity",
"type": "progene_text",
"text": [
"FliH"
],
"offsets": [
[
46,
50
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],
"normalized": []
},
{
"id": "split_0_train_1409_entity",
"type": "progene_text",
"text": [
"FliI"
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"offsets": [
[
53,
57
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],
"normalized": []
},
{
"id": "split_0_train_1410_entity",
"type": "progene_text",
"text": [
"FliJ"
],
"offsets": [
[
62,
66
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],
"normalized": []
},
{
"id": "split_0_train_1411_entity",
"type": "progene_text",
"text": [
"FlhAC"
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"offsets": [
[
153,
158
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],
"normalized": []
},
{
"id": "split_0_train_1412_entity",
"type": "progene_text",
"text": [
"FlhBC"
],
"offsets": [
[
163,
168
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1028 | split_0_train_1028 | [
{
"id": "split_0_train_1028_passage",
"type": "progene_text",
"text": [
"FliH , FlhAC and FliJ , when overproduced , caused inhibition of motility of wild - type cells and inhibition of the export of substrates such as the hook protein FlgE ."
],
"offsets": [
[
0,
169
]
]
}
]
| [
{
"id": "split_0_train_1413_entity",
"type": "progene_text",
"text": [
"FliH"
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"offsets": [
[
0,
4
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],
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},
{
"id": "split_0_train_1414_entity",
"type": "progene_text",
"text": [
"FlhAC"
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"offsets": [
[
7,
12
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],
"normalized": []
},
{
"id": "split_0_train_1415_entity",
"type": "progene_text",
"text": [
"FliJ"
],
"offsets": [
[
17,
21
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],
"normalized": []
},
{
"id": "split_0_train_1416_entity",
"type": "progene_text",
"text": [
"hook protein"
],
"offsets": [
[
150,
162
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],
"normalized": []
},
{
"id": "split_0_train_1417_entity",
"type": "progene_text",
"text": [
"FlgE"
],
"offsets": [
[
163,
167
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],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1029 | split_0_train_1029 | [
{
"id": "split_0_train_1029_passage",
"type": "progene_text",
"text": [
"Co - overproduction of FliH and FliI substantially relieved the inhibition caused by FliH , suggesting that it is excess free FliH that is inhibitory and that FliH and FliI form a complex ."
],
"offsets": [
[
0,
189
]
]
}
]
| [
{
"id": "split_0_train_1418_entity",
"type": "progene_text",
"text": [
"FliH"
],
"offsets": [
[
23,
27
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],
"normalized": []
},
{
"id": "split_0_train_1419_entity",
"type": "progene_text",
"text": [
"FliI"
],
"offsets": [
[
32,
36
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],
"normalized": []
},
{
"id": "split_0_train_1420_entity",
"type": "progene_text",
"text": [
"FliH"
],
"offsets": [
[
85,
89
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],
"normalized": []
},
{
"id": "split_0_train_1421_entity",
"type": "progene_text",
"text": [
"FliH"
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"offsets": [
[
126,
130
]
],
"normalized": []
},
{
"id": "split_0_train_1422_entity",
"type": "progene_text",
"text": [
"FliH"
],
"offsets": [
[
159,
163
]
],
"normalized": []
},
{
"id": "split_0_train_1423_entity",
"type": "progene_text",
"text": [
"FliI"
],
"offsets": [
[
168,
172
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1030 | split_0_train_1030 | [
{
"id": "split_0_train_1030_passage",
"type": "progene_text",
"text": [
"We purified His-FLAG - tagged versions of : ( i ) export components FliH , FliI , FliJ , FlhAC and FlhBC ; ( ii ) rod / hook - type export substrates FlgB ( rod protein ) , FlgE ( hook protein ) , FlgD ( hook capping protein ) and FliE ( basal body protein ) ; and ( iii ) filament - type export substrates FlgK and FlgL ( hook - filament junction proteins ) and FliC ( flagellin ) ."
],
"offsets": [
[
0,
383
]
]
}
]
| [
{
"id": "split_0_train_1424_entity",
"type": "progene_text",
"text": [
"FliH"
],
"offsets": [
[
68,
72
]
],
"normalized": []
},
{
"id": "split_0_train_1425_entity",
"type": "progene_text",
"text": [
"FliI"
],
"offsets": [
[
75,
79
]
],
"normalized": []
},
{
"id": "split_0_train_1426_entity",
"type": "progene_text",
"text": [
"FliJ"
],
"offsets": [
[
82,
86
]
],
"normalized": []
},
{
"id": "split_0_train_1427_entity",
"type": "progene_text",
"text": [
"FlhAC"
],
"offsets": [
[
89,
94
]
],
"normalized": []
},
{
"id": "split_0_train_1428_entity",
"type": "progene_text",
"text": [
"FlhBC"
],
"offsets": [
[
99,
104
]
],
"normalized": []
},
{
"id": "split_0_train_1429_entity",
"type": "progene_text",
"text": [
"FlgB"
],
"offsets": [
[
150,
154
]
],
"normalized": []
},
{
"id": "split_0_train_1430_entity",
"type": "progene_text",
"text": [
"rod protein"
],
"offsets": [
[
157,
168
]
],
"normalized": []
},
{
"id": "split_0_train_1431_entity",
"type": "progene_text",
"text": [
"FlgE"
],
"offsets": [
[
173,
177
]
],
"normalized": []
},
{
"id": "split_0_train_1432_entity",
"type": "progene_text",
"text": [
"hook protein"
],
"offsets": [
[
180,
192
]
],
"normalized": []
},
{
"id": "split_0_train_1433_entity",
"type": "progene_text",
"text": [
"FlgD"
],
"offsets": [
[
197,
201
]
],
"normalized": []
},
{
"id": "split_0_train_1434_entity",
"type": "progene_text",
"text": [
"hook capping protein"
],
"offsets": [
[
204,
224
]
],
"normalized": []
},
{
"id": "split_0_train_1435_entity",
"type": "progene_text",
"text": [
"FliE"
],
"offsets": [
[
231,
235
]
],
"normalized": []
},
{
"id": "split_0_train_1436_entity",
"type": "progene_text",
"text": [
"basal body protein"
],
"offsets": [
[
238,
256
]
],
"normalized": []
},
{
"id": "split_0_train_1437_entity",
"type": "progene_text",
"text": [
"FlgK"
],
"offsets": [
[
307,
311
]
],
"normalized": []
},
{
"id": "split_0_train_1438_entity",
"type": "progene_text",
"text": [
"FlgL"
],
"offsets": [
[
316,
320
]
],
"normalized": []
},
{
"id": "split_0_train_1439_entity",
"type": "progene_text",
"text": [
"hook - filament junction proteins"
],
"offsets": [
[
323,
356
]
],
"normalized": []
},
{
"id": "split_0_train_1440_entity",
"type": "progene_text",
"text": [
"FliC"
],
"offsets": [
[
363,
367
]
],
"normalized": []
},
{
"id": "split_0_train_1441_entity",
"type": "progene_text",
"text": [
"flagellin"
],
"offsets": [
[
370,
379
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1031 | split_0_train_1031 | [
{
"id": "split_0_train_1031_passage",
"type": "progene_text",
"text": [
"We tested for protein - protein interactions by affinity blotting ."
],
"offsets": [
[
0,
67
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1032 | split_0_train_1032 | [
{
"id": "split_0_train_1032_passage",
"type": "progene_text",
"text": [
"In many cases , a given protein interacted with more than one other component , indicating that there are likely to be multiple dynamic interactions or interactions that involve more than two components ."
],
"offsets": [
[
0,
204
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1033 | split_0_train_1033 | [
{
"id": "split_0_train_1033_passage",
"type": "progene_text",
"text": [
"Interactions of FlhBC with rod / hook - type substrates were strong , whereas those with filament - type substrates were very weak ; this may reflect the role of FlhB in substrate specificity switching ."
],
"offsets": [
[
0,
203
]
]
}
]
| [
{
"id": "split_0_train_1442_entity",
"type": "progene_text",
"text": [
"FlhBC"
],
"offsets": [
[
16,
21
]
],
"normalized": []
},
{
"id": "split_0_train_1443_entity",
"type": "progene_text",
"text": [
"FlhB"
],
"offsets": [
[
162,
166
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1034 | split_0_train_1034 | [
{
"id": "split_0_train_1034_passage",
"type": "progene_text",
"text": [
"We propose a model for the flagellar export apparatus in which FlhA and FlhB and the other four integral membrane proteins of the apparatus form a complex at the base of the flagellar motor ."
],
"offsets": [
[
0,
191
]
]
}
]
| [
{
"id": "split_0_train_1444_entity",
"type": "progene_text",
"text": [
"FlhA"
],
"offsets": [
[
63,
67
]
],
"normalized": []
},
{
"id": "split_0_train_1445_entity",
"type": "progene_text",
"text": [
"FlhB"
],
"offsets": [
[
72,
76
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1035 | split_0_train_1035 | [
{
"id": "split_0_train_1035_passage",
"type": "progene_text",
"text": [
"A soluble complex of at least three proteins ( FliH , FliI and FliJ ) bind the protein to be exported and then interact with the complex at the motor to deliver the protein , which is then exported in an ATP - dependent process mediated by FliI ."
],
"offsets": [
[
0,
246
]
]
}
]
| [
{
"id": "split_0_train_1446_entity",
"type": "progene_text",
"text": [
"FliH"
],
"offsets": [
[
47,
51
]
],
"normalized": []
},
{
"id": "split_0_train_1447_entity",
"type": "progene_text",
"text": [
"FliI"
],
"offsets": [
[
54,
58
]
],
"normalized": []
},
{
"id": "split_0_train_1448_entity",
"type": "progene_text",
"text": [
"FliJ"
],
"offsets": [
[
63,
67
]
],
"normalized": []
},
{
"id": "split_0_train_1449_entity",
"type": "progene_text",
"text": [
"FliI"
],
"offsets": [
[
240,
244
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1036 | split_0_train_1036 | [
{
"id": "split_0_train_1036_passage",
"type": "progene_text",
"text": [
"Distribution of neurons immunoreactive for calcium - binding proteins varies across areas of cat primary somatosensory cortex ."
],
"offsets": [
[
0,
127
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1037 | split_0_train_1037 | [
{
"id": "split_0_train_1037_passage",
"type": "progene_text",
"text": [
"The primary somatosensory ( SI ) cortex in the cat contains four cytoarchitectonic areas that appear to contain separate body representations and have different functions ."
],
"offsets": [
[
0,
172
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1038 | split_0_train_1038 | [
{
"id": "split_0_train_1038_passage",
"type": "progene_text",
"text": [
"We tested whether functional differences among these areas are reflected in the densities of neurons containing each of three calcium - binding proteins : parvalbumin ( PV ) , calbindin ( CB ) , and calretinin ( CR ) ."
],
"offsets": [
[
0,
218
]
]
}
]
| [
{
"id": "split_0_train_1450_entity",
"type": "progene_text",
"text": [
"parvalbumin"
],
"offsets": [
[
155,
166
]
],
"normalized": []
},
{
"id": "split_0_train_1451_entity",
"type": "progene_text",
"text": [
"PV"
],
"offsets": [
[
169,
171
]
],
"normalized": []
},
{
"id": "split_0_train_1452_entity",
"type": "progene_text",
"text": [
"calbindin"
],
"offsets": [
[
176,
185
]
],
"normalized": []
},
{
"id": "split_0_train_1453_entity",
"type": "progene_text",
"text": [
"CB"
],
"offsets": [
[
188,
190
]
],
"normalized": []
},
{
"id": "split_0_train_1454_entity",
"type": "progene_text",
"text": [
"calretinin"
],
"offsets": [
[
199,
209
]
],
"normalized": []
},
{
"id": "split_0_train_1455_entity",
"type": "progene_text",
"text": [
"CR"
],
"offsets": [
[
212,
214
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1039 | split_0_train_1039 | [
{
"id": "split_0_train_1039_passage",
"type": "progene_text",
"text": [
"Colocalization experiments revealed that CR was localized in a population of neurons distinct from those containing PV or CB ."
],
"offsets": [
[
0,
126
]
]
}
]
| [
{
"id": "split_0_train_1456_entity",
"type": "progene_text",
"text": [
"CR"
],
"offsets": [
[
41,
43
]
],
"normalized": []
},
{
"id": "split_0_train_1457_entity",
"type": "progene_text",
"text": [
"PV"
],
"offsets": [
[
116,
118
]
],
"normalized": []
},
{
"id": "split_0_train_1458_entity",
"type": "progene_text",
"text": [
"CB"
],
"offsets": [
[
122,
124
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1040 | split_0_train_1040 | [
{
"id": "split_0_train_1040_passage",
"type": "progene_text",
"text": [
"The general laminar distributions of the three calcium - binding proteins were similar to those described in other species and cortical areas , but there were significant density differences in layers II and III across SI ."
],
"offsets": [
[
0,
223
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1041 | split_0_train_1041 | [
{
"id": "split_0_train_1041_passage",
"type": "progene_text",
"text": [
"The density of PV - immunoreactive neurons was higher in areas 3b and 1 than in areas 3a and 2 ."
],
"offsets": [
[
0,
96
]
]
}
]
| [
{
"id": "split_0_train_1459_entity",
"type": "progene_text",
"text": [
"PV"
],
"offsets": [
[
15,
17
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1042 | split_0_train_1042 | [
{
"id": "split_0_train_1042_passage",
"type": "progene_text",
"text": [
"CB - immunoreactive neurons were found in higher densities in anterior SI than in posterior SI , and the pattern of CR - immunoreactive neurons was reciprocal to that of CB , with significantly higher densities in posterior regions of SI ."
],
"offsets": [
[
0,
239
]
]
}
]
| [
{
"id": "split_0_train_1460_entity",
"type": "progene_text",
"text": [
"CB"
],
"offsets": [
[
0,
2
]
],
"normalized": []
},
{
"id": "split_0_train_1461_entity",
"type": "progene_text",
"text": [
"CR"
],
"offsets": [
[
116,
118
]
],
"normalized": []
},
{
"id": "split_0_train_1462_entity",
"type": "progene_text",
"text": [
"CB"
],
"offsets": [
[
170,
172
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1043 | split_0_train_1043 | [
{
"id": "split_0_train_1043_passage",
"type": "progene_text",
"text": [
"Since the firing characteristics of nonpyramidal neurons appear to be related to their calcium - binding protein content , differences in regional distributions of these neurons in layers II and III may contribute to functional differences between the cytoarchitectonic areas of SI cortex ."
],
"offsets": [
[
0,
290
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1044 | split_0_train_1044 | [
{
"id": "split_0_train_1044_passage",
"type": "progene_text",
"text": [
"Regulation of plasminogen activation by TGF-beta in cultured human retinal endothelial cells ."
],
"offsets": [
[
0,
94
]
]
}
]
| [
{
"id": "split_0_train_1463_entity",
"type": "progene_text",
"text": [
"plasminogen"
],
"offsets": [
[
14,
25
]
],
"normalized": []
},
{
"id": "split_0_train_1464_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
40,
48
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1045 | split_0_train_1045 | [
{
"id": "split_0_train_1045_passage",
"type": "progene_text",
"text": [
"BACKGROUND / AIMS :"
],
"offsets": [
[
0,
19
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1046 | split_0_train_1046 | [
{
"id": "split_0_train_1046_passage",
"type": "progene_text",
"text": [
"Regulation of plasmin mediated extracellular matrix degradation by vascular endothelial cells is important in the development of angiogenesis ."
],
"offsets": [
[
0,
143
]
]
}
]
| [
{
"id": "split_0_train_1465_entity",
"type": "progene_text",
"text": [
"plasmin"
],
"offsets": [
[
14,
21
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1047 | split_0_train_1047 | [
{
"id": "split_0_train_1047_passage",
"type": "progene_text",
"text": [
"The aim was to determine whether transforming growth factor beta ( TGF-beta ) affected the regulation of components of the plasminogen system by human retinal endothelial cells , in order to define more clearly the role of TGF-beta in retinal angiogenesis in the context of diabetes mellitus ."
],
"offsets": [
[
0,
293
]
]
}
]
| [
{
"id": "split_0_train_1466_entity",
"type": "progene_text",
"text": [
"transforming growth factor beta"
],
"offsets": [
[
33,
64
]
],
"normalized": []
},
{
"id": "split_0_train_1467_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
67,
75
]
],
"normalized": []
},
{
"id": "split_0_train_1468_entity",
"type": "progene_text",
"text": [
"plasminogen"
],
"offsets": [
[
123,
134
]
],
"normalized": []
},
{
"id": "split_0_train_1469_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
223,
231
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1048 | split_0_train_1048 | [
{
"id": "split_0_train_1048_passage",
"type": "progene_text",
"text": [
"METHODS :"
],
"offsets": [
[
0,
9
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1049 | split_0_train_1049 | [
{
"id": "split_0_train_1049_passage",
"type": "progene_text",
"text": [
"Human retinal endothelial cells ( HREC ) were isolated from donor eyes and used between passages 4-8 ."
],
"offsets": [
[
0,
102
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1050 | split_0_train_1050 | [
{
"id": "split_0_train_1050_passage",
"type": "progene_text",
"text": [
"The cells were cultured in medium supplemented with 2 , 5 , 15 , or 25 mM glucose , plus or minus TGF-beta ( 1 ng / ml ) ."
],
"offsets": [
[
0,
122
]
]
}
]
| [
{
"id": "split_0_train_1470_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
98,
106
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1051 | split_0_train_1051 | [
{
"id": "split_0_train_1051_passage",
"type": "progene_text",
"text": [
"The concentrations of tissue plasminogen activator (t-PA ) , urokinase plasminogen activator ( u-PA ) , and plasminogen activator inhibitor type 1 ( PAI-1 ) in cell conditioned medium were determined by ELISA and the level of PAI-1 mRNA was determined using northern hybridisation ."
],
"offsets": [
[
0,
282
]
]
}
]
| [
{
"id": "split_0_train_1471_entity",
"type": "progene_text",
"text": [
"tissue plasminogen activator"
],
"offsets": [
[
22,
50
]
],
"normalized": []
},
{
"id": "split_0_train_1472_entity",
"type": "progene_text",
"text": [
"(t-PA"
],
"offsets": [
[
51,
56
]
],
"normalized": []
},
{
"id": "split_0_train_1473_entity",
"type": "progene_text",
"text": [
"urokinase plasminogen activator"
],
"offsets": [
[
61,
92
]
],
"normalized": []
},
{
"id": "split_0_train_1474_entity",
"type": "progene_text",
"text": [
"u-PA"
],
"offsets": [
[
95,
99
]
],
"normalized": []
},
{
"id": "split_0_train_1475_entity",
"type": "progene_text",
"text": [
"plasminogen activator inhibitor type 1"
],
"offsets": [
[
108,
146
]
],
"normalized": []
},
{
"id": "split_0_train_1476_entity",
"type": "progene_text",
"text": [
"PAI-1"
],
"offsets": [
[
149,
154
]
],
"normalized": []
},
{
"id": "split_0_train_1477_entity",
"type": "progene_text",
"text": [
"PAI-1"
],
"offsets": [
[
226,
231
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1052 | split_0_train_1052 | [
{
"id": "split_0_train_1052_passage",
"type": "progene_text",
"text": [
"Cell associated plasminogen activity was determined using a clot lysis assay and a chromogenic assay ."
],
"offsets": [
[
0,
102
]
]
}
]
| [
{
"id": "split_0_train_1478_entity",
"type": "progene_text",
"text": [
"plasminogen"
],
"offsets": [
[
16,
27
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1053 | split_0_train_1053 | [
{
"id": "split_0_train_1053_passage",
"type": "progene_text",
"text": [
"RESULTS :"
],
"offsets": [
[
0,
9
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1054 | split_0_train_1054 | [
{
"id": "split_0_train_1054_passage",
"type": "progene_text",
"text": [
"Under basal conditions ( 5 mM glucose ) , HREC produced PAI-1 , t-PA , and trace amounts of u-PA ."
],
"offsets": [
[
0,
98
]
]
}
]
| [
{
"id": "split_0_train_1479_entity",
"type": "progene_text",
"text": [
"PAI-1"
],
"offsets": [
[
56,
61
]
],
"normalized": []
},
{
"id": "split_0_train_1480_entity",
"type": "progene_text",
"text": [
"t-PA"
],
"offsets": [
[
64,
68
]
],
"normalized": []
},
{
"id": "split_0_train_1481_entity",
"type": "progene_text",
"text": [
"u-PA"
],
"offsets": [
[
92,
96
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1055 | split_0_train_1055 | [
{
"id": "split_0_train_1055_passage",
"type": "progene_text",
"text": [
"Cell surface plasminogen activation observed by lysis of fibrin or by cleavage of chromogenic substrate , was mediated by t-PA ."
],
"offsets": [
[
0,
128
]
]
}
]
| [
{
"id": "split_0_train_1482_entity",
"type": "progene_text",
"text": [
"fibrin"
],
"offsets": [
[
57,
63
]
],
"normalized": []
},
{
"id": "split_0_train_1483_entity",
"type": "progene_text",
"text": [
"t-PA"
],
"offsets": [
[
122,
126
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1056 | split_0_train_1056 | [
{
"id": "split_0_train_1056_passage",
"type": "progene_text",
"text": [
"Glucose at varying concentrations ( 2-25 mM ) had no significant effect on t-PA mediated clot lysis ."
],
"offsets": [
[
0,
101
]
]
}
]
| [
{
"id": "split_0_train_1484_entity",
"type": "progene_text",
"text": [
"t-PA"
],
"offsets": [
[
75,
79
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1057 | split_0_train_1057 | [
{
"id": "split_0_train_1057_passage",
"type": "progene_text",
"text": [
"In contrast , treatment with TGF-beta resulted in increased synthesis of PAI-1 protein and mRNA ."
],
"offsets": [
[
0,
97
]
]
}
]
| [
{
"id": "split_0_train_1485_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
29,
37
]
],
"normalized": []
},
{
"id": "split_0_train_1486_entity",
"type": "progene_text",
"text": [
"PAI-1"
],
"offsets": [
[
73,
78
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1058 | split_0_train_1058 | [
{
"id": "split_0_train_1058_passage",
"type": "progene_text",
"text": [
"The increased expression of the PAI-1 mRNAs by TGF-beta did not occur uniformly , the 2.3 kb mRNA transcript was preferentially increased in comparison with the 3.2 kb mRNA ( p < 0.05 ) ."
],
"offsets": [
[
0,
187
]
]
}
]
| [
{
"id": "split_0_train_1487_entity",
"type": "progene_text",
"text": [
"PAI-1"
],
"offsets": [
[
32,
37
]
],
"normalized": []
},
{
"id": "split_0_train_1488_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
47,
55
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1059 | split_0_train_1059 | [
{
"id": "split_0_train_1059_passage",
"type": "progene_text",
"text": [
"CONCLUSIONS :"
],
"offsets": [
[
0,
13
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1060 | split_0_train_1060 | [
{
"id": "split_0_train_1060_passage",
"type": "progene_text",
"text": [
"These data demonstrate that TGF-beta increases PAI-1 and decreases cell associated lysis ."
],
"offsets": [
[
0,
90
]
]
}
]
| [
{
"id": "split_0_train_1489_entity",
"type": "progene_text",
"text": [
"TGF-beta"
],
"offsets": [
[
28,
36
]
],
"normalized": []
},
{
"id": "split_0_train_1490_entity",
"type": "progene_text",
"text": [
"PAI-1"
],
"offsets": [
[
47,
52
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1061 | split_0_train_1061 | [
{
"id": "split_0_train_1061_passage",
"type": "progene_text",
"text": [
"This is sufficient to decrease the normal lytic potential of HREC ."
],
"offsets": [
[
0,
67
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1062 | split_0_train_1062 | [
{
"id": "split_0_train_1062_passage",
"type": "progene_text",
"text": [
"Molecular cloning and characterization of mouse CD97 ."
],
"offsets": [
[
0,
54
]
]
}
]
| [
{
"id": "split_0_train_1491_entity",
"type": "progene_text",
"text": [
"CD97"
],
"offsets": [
[
48,
52
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1063 | split_0_train_1063 | [
{
"id": "split_0_train_1063_passage",
"type": "progene_text",
"text": [
"The EGF-TM7 family ( CD97 and EMR1 ) is a group of class II seven - span transmembrane receptors predominantly expressed by cells of the immune system ."
],
"offsets": [
[
0,
152
]
]
}
]
| [
{
"id": "split_0_train_1492_entity",
"type": "progene_text",
"text": [
"EGF-TM7 family"
],
"offsets": [
[
4,
18
]
],
"normalized": []
},
{
"id": "split_0_train_1493_entity",
"type": "progene_text",
"text": [
"CD97"
],
"offsets": [
[
21,
25
]
],
"normalized": []
},
{
"id": "split_0_train_1494_entity",
"type": "progene_text",
"text": [
"EMR1"
],
"offsets": [
[
30,
34
]
],
"normalized": []
},
{
"id": "split_0_train_1495_entity",
"type": "progene_text",
"text": [
"seven - span transmembrane receptors"
],
"offsets": [
[
60,
96
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1064 | split_0_train_1064 | [
{
"id": "split_0_train_1064_passage",
"type": "progene_text",
"text": [
"Recently , we have identified CD55 , a regulatory molecule of the complement cascade , as a cellular ligand of human CD97 ( hCD97 ) ."
],
"offsets": [
[
0,
133
]
]
}
]
| [
{
"id": "split_0_train_1496_entity",
"type": "progene_text",
"text": [
"CD55"
],
"offsets": [
[
30,
34
]
],
"normalized": []
},
{
"id": "split_0_train_1497_entity",
"type": "progene_text",
"text": [
"CD97"
],
"offsets": [
[
117,
121
]
],
"normalized": []
},
{
"id": "split_0_train_1498_entity",
"type": "progene_text",
"text": [
"hCD97"
],
"offsets": [
[
124,
129
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1065 | split_0_train_1065 | [
{
"id": "split_0_train_1065_passage",
"type": "progene_text",
"text": [
"In this study , the molecular properties of mouse CD97 ( mCD97 ) are described ."
],
"offsets": [
[
0,
80
]
]
}
]
| [
{
"id": "split_0_train_1499_entity",
"type": "progene_text",
"text": [
"CD97"
],
"offsets": [
[
50,
54
]
],
"normalized": []
},
{
"id": "split_0_train_1500_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
57,
62
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1066 | split_0_train_1066 | [
{
"id": "split_0_train_1066_passage",
"type": "progene_text",
"text": [
"Like hCD97 , mCD97 has an extended extracellular region with several epidermal growth factor - like ( EGF ) domains ."
],
"offsets": [
[
0,
117
]
]
}
]
| [
{
"id": "split_0_train_1501_entity",
"type": "progene_text",
"text": [
"hCD97"
],
"offsets": [
[
5,
10
]
],
"normalized": []
},
{
"id": "split_0_train_1502_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
13,
18
]
],
"normalized": []
},
{
"id": "split_0_train_1503_entity",
"type": "progene_text",
"text": [
"epidermal growth factor"
],
"offsets": [
[
69,
92
]
],
"normalized": []
},
{
"id": "split_0_train_1504_entity",
"type": "progene_text",
"text": [
"EGF"
],
"offsets": [
[
102,
105
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1067 | split_0_train_1067 | [
{
"id": "split_0_train_1067_passage",
"type": "progene_text",
"text": [
"Due to alternative RNA splicing , isoforms with three and four EGF domains exist , designated mCD97 ( EGF1 , 2,4 ) and mCD97 ( EGF1 , 2 , 3,4 ) respectively ."
],
"offsets": [
[
0,
158
]
]
}
]
| [
{
"id": "split_0_train_1505_entity",
"type": "progene_text",
"text": [
"EGF"
],
"offsets": [
[
63,
66
]
],
"normalized": []
},
{
"id": "split_0_train_1506_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
94,
99
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1068 | split_0_train_1068 | [
{
"id": "split_0_train_1068_passage",
"type": "progene_text",
"text": [
"All EGF domains , except for the N - terminal one , possess a calcium - binding site ."
],
"offsets": [
[
0,
86
]
]
}
]
| [
{
"id": "split_0_train_1507_entity",
"type": "progene_text",
"text": [
"EGF"
],
"offsets": [
[
4,
7
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1069 | split_0_train_1069 | [
{
"id": "split_0_train_1069_passage",
"type": "progene_text",
"text": [
"In a third isoform mCD97 ( EGF1,2,X,3,4 ) , a sequence of 45 amino acids was found between the second and third EGF domain that does not correspond to any known protein module ."
],
"offsets": [
[
0,
177
]
]
}
]
| [
{
"id": "split_0_train_1508_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
19,
24
]
],
"normalized": []
},
{
"id": "split_0_train_1509_entity",
"type": "progene_text",
"text": [
"EGF"
],
"offsets": [
[
112,
115
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1070 | split_0_train_1070 | [
{
"id": "split_0_train_1070_passage",
"type": "progene_text",
"text": [
"Using newly generated mCD97 mAb , we show that analogous to the blood expression pattern of hCD97 , mCD97 can be found on lymphoid and myeloid cells ."
],
"offsets": [
[
0,
150
]
]
}
]
| [
{
"id": "split_0_train_1510_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
22,
27
]
],
"normalized": []
},
{
"id": "split_0_train_1511_entity",
"type": "progene_text",
"text": [
"hCD97"
],
"offsets": [
[
92,
97
]
],
"normalized": []
},
{
"id": "split_0_train_1512_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
100,
105
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1071 | split_0_train_1071 | [
{
"id": "split_0_train_1071_passage",
"type": "progene_text",
"text": [
"Adhesion of mouse erythrocytes and splenocytes to COS cells expressing mCD97 ( EGF1,2,4 ) or mCD97 ( EGF1 , 2 , 3 , 4 ) could be blocked by mouse CD55 ( mCD55 ) antibody , identifying mCD55 as a cellular ligand for mCD97 ."
],
"offsets": [
[
0,
222
]
]
}
]
| [
{
"id": "split_0_train_1513_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
71,
76
]
],
"normalized": []
},
{
"id": "split_0_train_1514_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
93,
98
]
],
"normalized": []
},
{
"id": "split_0_train_1515_entity",
"type": "progene_text",
"text": [
"CD55"
],
"offsets": [
[
146,
150
]
],
"normalized": []
},
{
"id": "split_0_train_1516_entity",
"type": "progene_text",
"text": [
"mCD55"
],
"offsets": [
[
153,
158
]
],
"normalized": []
},
{
"id": "split_0_train_1517_entity",
"type": "progene_text",
"text": [
"mCD55"
],
"offsets": [
[
184,
189
]
],
"normalized": []
},
{
"id": "split_0_train_1518_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
215,
220
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1072 | split_0_train_1072 | [
{
"id": "split_0_train_1072_passage",
"type": "progene_text",
"text": [
"Consistent with the necessity of directly linked EGF domains for the integrity of the CD55 - binding site on hCD97 , no adhesion was detected to the largest mouse isoform mCD97 ( EGF1 , 2 , X,3,4 ) ."
],
"offsets": [
[
0,
199
]
]
}
]
| [
{
"id": "split_0_train_1519_entity",
"type": "progene_text",
"text": [
"EGF"
],
"offsets": [
[
49,
52
]
],
"normalized": []
},
{
"id": "split_0_train_1520_entity",
"type": "progene_text",
"text": [
"CD55"
],
"offsets": [
[
86,
90
]
],
"normalized": []
},
{
"id": "split_0_train_1521_entity",
"type": "progene_text",
"text": [
"hCD97"
],
"offsets": [
[
109,
114
]
],
"normalized": []
},
{
"id": "split_0_train_1522_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
171,
176
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1073 | split_0_train_1073 | [
{
"id": "split_0_train_1073_passage",
"type": "progene_text",
"text": [
"Remarkably , we found that the interaction between CD97 and CD55 is phylogenetically restricted , as indicated by the selective adhesion of primate erythrocytes to hCD97 transfectants , and of mouse and rat erythrocytes to mCD97 transfectants respectively ."
],
"offsets": [
[
0,
257
]
]
}
]
| [
{
"id": "split_0_train_1523_entity",
"type": "progene_text",
"text": [
"CD97"
],
"offsets": [
[
51,
55
]
],
"normalized": []
},
{
"id": "split_0_train_1524_entity",
"type": "progene_text",
"text": [
"CD55"
],
"offsets": [
[
60,
64
]
],
"normalized": []
},
{
"id": "split_0_train_1525_entity",
"type": "progene_text",
"text": [
"hCD97"
],
"offsets": [
[
164,
169
]
],
"normalized": []
},
{
"id": "split_0_train_1526_entity",
"type": "progene_text",
"text": [
"mCD97"
],
"offsets": [
[
223,
228
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1074 | split_0_train_1074 | [
{
"id": "split_0_train_1074_passage",
"type": "progene_text",
"text": [
"Regulation of expression of the human beta-1,2-N-acetylglucosaminyltransferase II gene ( MGAT2 ) by Ets transcription factors ."
],
"offsets": [
[
0,
127
]
]
}
]
| [
{
"id": "split_0_train_1527_entity",
"type": "progene_text",
"text": [
"beta-1,2-N-acetylglucosaminyltransferase II"
],
"offsets": [
[
38,
81
]
],
"normalized": []
},
{
"id": "split_0_train_1528_entity",
"type": "progene_text",
"text": [
"MGAT2"
],
"offsets": [
[
89,
94
]
],
"normalized": []
},
{
"id": "split_0_train_1529_entity",
"type": "progene_text",
"text": [
"Ets"
],
"offsets": [
[
100,
103
]
],
"normalized": []
},
{
"id": "split_0_train_1530_entity",
"type": "progene_text",
"text": [
"transcription factors"
],
"offsets": [
[
104,
125
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1075 | split_0_train_1075 | [
{
"id": "split_0_train_1075_passage",
"type": "progene_text",
"text": [
"Oncogenic transformation of fibroblasts by the src oncogene has long been known to cause an increase in the size of cell - surface protein - bound oligosaccharides , owing primarily to increased N - glycan branching mediated by increased beta-1,6-N-acetylglucosaminyltransferase V ( GnT V ) activity ."
],
"offsets": [
[
0,
301
]
]
}
]
| [
{
"id": "split_0_train_1531_entity",
"type": "progene_text",
"text": [
"src"
],
"offsets": [
[
47,
50
]
],
"normalized": []
},
{
"id": "split_0_train_1532_entity",
"type": "progene_text",
"text": [
"beta-1,6-N-acetylglucosaminyltransferase V"
],
"offsets": [
[
238,
280
]
],
"normalized": []
},
{
"id": "split_0_train_1533_entity",
"type": "progene_text",
"text": [
"GnT V"
],
"offsets": [
[
283,
288
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1076 | split_0_train_1076 | [
{
"id": "split_0_train_1076_passage",
"type": "progene_text",
"text": [
"The src - responsive element of the GnT V promoter was localized to Ets - binding sites and the promoter was transcriptionally stimulated by both ets-1 and ets-2 expression [ Buckhaults , Chen , Fregien and Pierce ( 1997 ) J. Biol. Chem. 272 , 19575 - 19581 ; Kang , Saito , Ihara , Miyoshi , Koyama , Sheng and Taniguchi ( 1996 ) J. Biol. Chem. 271 , 26706 - 26712 ] ."
],
"offsets": [
[
0,
369
]
]
}
]
| [
{
"id": "split_0_train_1534_entity",
"type": "progene_text",
"text": [
"src"
],
"offsets": [
[
4,
7
]
],
"normalized": []
},
{
"id": "split_0_train_1535_entity",
"type": "progene_text",
"text": [
"GnT V"
],
"offsets": [
[
36,
41
]
],
"normalized": []
},
{
"id": "split_0_train_1536_entity",
"type": "progene_text",
"text": [
"Ets"
],
"offsets": [
[
68,
71
]
],
"normalized": []
},
{
"id": "split_0_train_1537_entity",
"type": "progene_text",
"text": [
"ets-1"
],
"offsets": [
[
146,
151
]
],
"normalized": []
},
{
"id": "split_0_train_1538_entity",
"type": "progene_text",
"text": [
"ets-2"
],
"offsets": [
[
156,
161
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1077 | split_0_train_1077 | [
{
"id": "split_0_train_1077_passage",
"type": "progene_text",
"text": [
"Because GnT V action requires the prior action of beta-1,2-N-acetylglucosaminyltransferase II ( GnT II ) and the human GnT II promoter contains four putative Ets - binding sites [ Chen , Zhou , Tan and Schachter ( 1998 ) Glycoconj. J. 15 , 301 - 308 ] , GnT II might also be under oncogenic control via Ets transcription factors ."
],
"offsets": [
[
0,
330
]
]
}
]
| [
{
"id": "split_0_train_1539_entity",
"type": "progene_text",
"text": [
"GnT V"
],
"offsets": [
[
8,
13
]
],
"normalized": []
},
{
"id": "split_0_train_1540_entity",
"type": "progene_text",
"text": [
"beta-1,2-N-acetylglucosaminyltransferase II"
],
"offsets": [
[
50,
93
]
],
"normalized": []
},
{
"id": "split_0_train_1541_entity",
"type": "progene_text",
"text": [
"GnT II"
],
"offsets": [
[
96,
102
]
],
"normalized": []
},
{
"id": "split_0_train_1542_entity",
"type": "progene_text",
"text": [
"GnT II"
],
"offsets": [
[
119,
125
]
],
"normalized": []
},
{
"id": "split_0_train_1543_entity",
"type": "progene_text",
"text": [
"Ets"
],
"offsets": [
[
158,
161
]
],
"normalized": []
},
{
"id": "split_0_train_1544_entity",
"type": "progene_text",
"text": [
"GnT II"
],
"offsets": [
[
254,
260
]
],
"normalized": []
},
{
"id": "split_0_train_1545_entity",
"type": "progene_text",
"text": [
"Ets"
],
"offsets": [
[
303,
306
]
],
"normalized": []
},
{
"id": "split_0_train_1546_entity",
"type": "progene_text",
"text": [
"transcription factors"
],
"offsets": [
[
307,
328
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1078 | split_0_train_1078 | [
{
"id": "split_0_train_1078_passage",
"type": "progene_text",
"text": [
"We now report that co - transfection into HepG2 or COS-1 cells of either ets-1 or ets-2 expression plasmids together with chimaeric GnT II promoter - chloramphenicol acetyltransferase plasmids results in a 2 - 4 - fold stimulation of promoter activity ."
],
"offsets": [
[
0,
253
]
]
}
]
| [
{
"id": "split_0_train_1547_entity",
"type": "progene_text",
"text": [
"ets-1"
],
"offsets": [
[
73,
78
]
],
"normalized": []
},
{
"id": "split_0_train_1548_entity",
"type": "progene_text",
"text": [
"ets-2"
],
"offsets": [
[
82,
87
]
],
"normalized": []
},
{
"id": "split_0_train_1549_entity",
"type": "progene_text",
"text": [
"GnT II"
],
"offsets": [
[
132,
138
]
],
"normalized": []
},
{
"id": "split_0_train_1550_entity",
"type": "progene_text",
"text": [
"chloramphenicol acetyltransferase"
],
"offsets": [
[
150,
183
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1079 | split_0_train_1079 | [
{
"id": "split_0_train_1079_passage",
"type": "progene_text",
"text": [
"Mobility - shift assays and South - Western blots localized the functional Ets - binding site to one of the four putative sites on the GnT II promoter ."
],
"offsets": [
[
0,
152
]
]
}
]
| [
{
"id": "split_0_train_1551_entity",
"type": "progene_text",
"text": [
"Ets"
],
"offsets": [
[
75,
78
]
],
"normalized": []
},
{
"id": "split_0_train_1552_entity",
"type": "progene_text",
"text": [
"GnT II"
],
"offsets": [
[
135,
141
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1080 | split_0_train_1080 | [
{
"id": "split_0_train_1080_passage",
"type": "progene_text",
"text": [
"The GnT II promoter , unlike the GnT V promoter , is not activated by either src or neu ."
],
"offsets": [
[
0,
89
]
]
}
]
| [
{
"id": "split_0_train_1553_entity",
"type": "progene_text",
"text": [
"GnT II"
],
"offsets": [
[
4,
10
]
],
"normalized": []
},
{
"id": "split_0_train_1554_entity",
"type": "progene_text",
"text": [
"GnT V"
],
"offsets": [
[
33,
38
]
],
"normalized": []
},
{
"id": "split_0_train_1555_entity",
"type": "progene_text",
"text": [
"src"
],
"offsets": [
[
77,
80
]
],
"normalized": []
},
{
"id": "split_0_train_1556_entity",
"type": "progene_text",
"text": [
"neu"
],
"offsets": [
[
84,
87
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1081 | split_0_train_1081 | [
{
"id": "split_0_train_1081_passage",
"type": "progene_text",
"text": [
"Therefore although both promoters are stimulated by a member of the Ets family of transcription factors , the functional role of this Ets transcriptional control seems to be different for the two genes ."
],
"offsets": [
[
0,
203
]
]
}
]
| [
{
"id": "split_0_train_1557_entity",
"type": "progene_text",
"text": [
"Ets family"
],
"offsets": [
[
68,
78
]
],
"normalized": []
},
{
"id": "split_0_train_1558_entity",
"type": "progene_text",
"text": [
"transcription factors"
],
"offsets": [
[
82,
103
]
],
"normalized": []
},
{
"id": "split_0_train_1559_entity",
"type": "progene_text",
"text": [
"Ets"
],
"offsets": [
[
134,
137
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1082 | split_0_train_1082 | [
{
"id": "split_0_train_1082_passage",
"type": "progene_text",
"text": [
"Alterations in cathepsin H activity and protein patterns in human colorectal carcinomas ."
],
"offsets": [
[
0,
89
]
]
}
]
| [
{
"id": "split_0_train_1560_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
15,
26
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1083 | split_0_train_1083 | [
{
"id": "split_0_train_1083_passage",
"type": "progene_text",
"text": [
"Our analyses of cathepsin H activity levels and protein forms in human colorectal cancers compared to matched control mucosa support the concept that altered proteinase expression patterns may reflect both cancer stage and site ."
],
"offsets": [
[
0,
229
]
]
}
]
| [
{
"id": "split_0_train_1561_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
16,
27
]
],
"normalized": []
},
{
"id": "split_0_train_1562_entity",
"type": "progene_text",
"text": [
"proteinase"
],
"offsets": [
[
158,
168
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1084 | split_0_train_1084 | [
{
"id": "split_0_train_1084_passage",
"type": "progene_text",
"text": [
"Cathepsin H - specific activity was significantly increased in colorectal cancers compared to control mucosa ( P = 0.003 ; n = 77 ) ."
],
"offsets": [
[
0,
133
]
]
}
]
| [
{
"id": "split_0_train_1563_entity",
"type": "progene_text",
"text": [
"Cathepsin H"
],
"offsets": [
[
0,
11
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1085 | split_0_train_1085 | [
{
"id": "split_0_train_1085_passage",
"type": "progene_text",
"text": [
"Highest specific activities and cancer / normal ratios ( C / N ) for activity were measured in Dukes ' B and C stage carcinomas , cancers involved in local spread and invasion to lymph nodes ."
],
"offsets": [
[
0,
192
]
]
}
]
| []
| []
| []
| []
|
split_0_train_1086 | split_0_train_1086 | [
{
"id": "split_0_train_1086_passage",
"type": "progene_text",
"text": [
"In contrast , cathepsin B and L activities analysed in the same paired extracts had been shown to be most frequently elevated in earlier stage carcinomas ( Dukes ' A and B ) , confirming that cathepsin H demonstrates a distinct pattern of expression during colorectal cancer progression ."
],
"offsets": [
[
0,
288
]
]
}
]
| [
{
"id": "split_0_train_1564_entity",
"type": "progene_text",
"text": [
"cathepsin B and L"
],
"offsets": [
[
14,
31
]
],
"normalized": []
},
{
"id": "split_0_train_1565_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
192,
203
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1087 | split_0_train_1087 | [
{
"id": "split_0_train_1087_passage",
"type": "progene_text",
"text": [
"Although cathepsin H activities were most commonly elevated in Dukes ' C cancers at all colon sites , both specific activity and C / N ratios were significantly higher for cancers of the left colon compared to other colon locations ."
],
"offsets": [
[
0,
233
]
]
}
]
| [
{
"id": "split_0_train_1566_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
9,
20
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1088 | split_0_train_1088 | [
{
"id": "split_0_train_1088_passage",
"type": "progene_text",
"text": [
"A subset of 43 paired extracts analysed on Western blots also revealed consistent changes in cathepsin H protein forms in cancers ."
],
"offsets": [
[
0,
131
]
]
}
]
| [
{
"id": "split_0_train_1567_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
93,
104
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1089 | split_0_train_1089 | [
{
"id": "split_0_train_1089_passage",
"type": "progene_text",
"text": [
"Normal mucosa typically showed a strong protein doublet at 31 and 29 kDa while cancers demonstrated decreased expression or total loss of the 31 kDa protein ( 90 % of cases ) , equal or increased expression of the 29 - kDa protein ( 67 % of cases ) and the new appearance or up - regulation of a cathepsin H band at 22 kDa ( 78 % of cases ) ."
],
"offsets": [
[
0,
342
]
]
}
]
| [
{
"id": "split_0_train_1568_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
296,
307
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1090 | split_0_train_1090 | [
{
"id": "split_0_train_1090_passage",
"type": "progene_text",
"text": [
"C / N ratios for cathepsin H enzyme activity correlated significantly with C / N ratios for the 29 kDa mature single - chain protein form ( P < 0.001 ) , with increased activity most commonly associated with elevated expression of 29 - kDa cathepsin H but also with up - regulation of the 22 - kDa band , suggesting a shift to more fully processed , mature active cathepsin H protein forms in cancers ."
],
"offsets": [
[
0,
402
]
]
}
]
| [
{
"id": "split_0_train_1569_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
17,
28
]
],
"normalized": []
},
{
"id": "split_0_train_1570_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
240,
251
]
],
"normalized": []
},
{
"id": "split_0_train_1571_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
364,
375
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1091 | split_0_train_1091 | [
{
"id": "split_0_train_1091_passage",
"type": "progene_text",
"text": [
"Changes in cathepsin H expression were also detected by immunohistochemistry as elevated cathepsin H staining in tumour epithelial cells ."
],
"offsets": [
[
0,
138
]
]
}
]
| [
{
"id": "split_0_train_1572_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
11,
22
]
],
"normalized": []
},
{
"id": "split_0_train_1573_entity",
"type": "progene_text",
"text": [
"cathepsin H"
],
"offsets": [
[
89,
100
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1092 | split_0_train_1092 | [
{
"id": "split_0_train_1092_passage",
"type": "progene_text",
"text": [
"Tunicamycin enhances the anticellular activity of interferon by inhibiting G1 / S phase progression in 3T3 cells ."
],
"offsets": [
[
0,
114
]
]
}
]
| [
{
"id": "split_0_train_1574_entity",
"type": "progene_text",
"text": [
"interferon"
],
"offsets": [
[
50,
60
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1093 | split_0_train_1093 | [
{
"id": "split_0_train_1093_passage",
"type": "progene_text",
"text": [
"We have shown earlier that the cell growth inhibitory activity of interferon ( IFN ) is significantly enhanced by tunicamycin ( TM ) ( Maheshwari et al. , Science 219 , 1339 - 1341 , 1983 ) ."
],
"offsets": [
[
0,
191
]
]
}
]
| [
{
"id": "split_0_train_1575_entity",
"type": "progene_text",
"text": [
"interferon"
],
"offsets": [
[
66,
76
]
],
"normalized": []
},
{
"id": "split_0_train_1576_entity",
"type": "progene_text",
"text": [
"IFN"
],
"offsets": [
[
79,
82
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1094 | split_0_train_1094 | [
{
"id": "split_0_train_1094_passage",
"type": "progene_text",
"text": [
"In this report , we investigated various regulatory points of synergistic action between TM and IFN-alpha / beta that inhibit cell growth in NIH 3T3 cells ."
],
"offsets": [
[
0,
156
]
]
}
]
| [
{
"id": "split_0_train_1577_entity",
"type": "progene_text",
"text": [
"IFN-alpha / beta"
],
"offsets": [
[
96,
112
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1095 | split_0_train_1095 | [
{
"id": "split_0_train_1095_passage",
"type": "progene_text",
"text": [
"The MTT ( 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide ) viability assays showed a dose - dependent increase in percentage inhibition of the cells when treated with either TM or IFN ."
],
"offsets": [
[
0,
200
]
]
}
]
| [
{
"id": "split_0_train_1578_entity",
"type": "progene_text",
"text": [
"IFN"
],
"offsets": [
[
195,
198
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1096 | split_0_train_1096 | [
{
"id": "split_0_train_1096_passage",
"type": "progene_text",
"text": [
"When doses of TM and IFN that had no significant inhibition on cell viability were used in combination , there was a pronounced suppression of DNA synthesis ( tritiated thymidine incorporation ) ."
],
"offsets": [
[
0,
196
]
]
}
]
| [
{
"id": "split_0_train_1579_entity",
"type": "progene_text",
"text": [
"IFN"
],
"offsets": [
[
21,
24
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1097 | split_0_train_1097 | [
{
"id": "split_0_train_1097_passage",
"type": "progene_text",
"text": [
"Flow cytometry studies revealed that individual treatments with either IFN or TM that did not alter the cell cycle profile , when combined , resulted in an impaired cell cycle by inhibiting G1 / S progression ."
],
"offsets": [
[
0,
210
]
]
}
]
| [
{
"id": "split_0_train_1580_entity",
"type": "progene_text",
"text": [
"IFN"
],
"offsets": [
[
71,
74
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1098 | split_0_train_1098 | [
{
"id": "split_0_train_1098_passage",
"type": "progene_text",
"text": [
"The blockage of G1 / S transition was associated with reduction of cyclin - dependent kinase ( CDK4 ) activity ."
],
"offsets": [
[
0,
112
]
]
}
]
| [
{
"id": "split_0_train_1581_entity",
"type": "progene_text",
"text": [
"cyclin - dependent kinase"
],
"offsets": [
[
67,
92
]
],
"normalized": []
},
{
"id": "split_0_train_1582_entity",
"type": "progene_text",
"text": [
"CDK4"
],
"offsets": [
[
95,
99
]
],
"normalized": []
}
]
| []
| []
| []
|
split_0_train_1099 | split_0_train_1099 | [
{
"id": "split_0_train_1099_passage",
"type": "progene_text",
"text": [
"The mRNA ( analyzed by ribonuclease protection assay ) and protein levels ( assayed by Western blotting ) of cyclins D1 , D3 , and CDK4 were downregulated by combined treatment with IFN and TM ."
],
"offsets": [
[
0,
194
]
]
}
]
| [
{
"id": "split_0_train_1583_entity",
"type": "progene_text",
"text": [
"ribonuclease"
],
"offsets": [
[
23,
35
]
],
"normalized": []
},
{
"id": "split_0_train_1584_entity",
"type": "progene_text",
"text": [
"cyclins D1 , D3"
],
"offsets": [
[
109,
124
]
],
"normalized": []
},
{
"id": "split_0_train_1585_entity",
"type": "progene_text",
"text": [
"CDK4"
],
"offsets": [
[
131,
135
]
],
"normalized": []
},
{
"id": "split_0_train_1586_entity",
"type": "progene_text",
"text": [
"IFN"
],
"offsets": [
[
182,
185
]
],
"normalized": []
}
]
| []
| []
| []
|
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