PubMed:15200408 / 1636-1844 JSONTXT

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LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
921 130-136 GeneOrGeneProduct denotes UP III NCBIGene:7380
922 145-148 DiseaseOrPhenotypicFeature denotes VUR MESH:C564042

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T14 0-208 Sentence denotes Studies of additional cases yielded a second set of data that, in combination with the first set, confirmed a weak association of UP III SNP7 in VUR (P= 0.036 adjusted for both subsets of cases vs. controls).

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T36 22-27 GeneOrGeneProduct denotes cases
T37 28-35 GeneOrGeneProduct denotes yielded
T38 110-114 GeneOrGeneProduct denotes weak
T39 130-136 GeneOrGeneProduct denotes UP III
T40 145-148 GeneOrGeneProduct denotes VUR
T41 188-193 GeneOrGeneProduct denotes cases

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T22 110-114 GeneOrGeneProduct denotes weak
T23 130-136 GeneOrGeneProduct denotes UP III
T24 145-148 GeneOrGeneProduct denotes VUR

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T17 145-148 DiseaseOrPhenotypicFeature denotes VUR D014718

LitCoin-GeneOrGeneProduct-v3

Id Subject Object Predicate Lexical cue
T6 130-136 GeneOrGeneProduct denotes UP III

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T25 145-148 DiseaseOrPhenotypicFeature denotes VUR 0008653|0006007

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T18 145-148 DiseaseOrPhenotypicFeature denotes VUR D014718

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T17 145-148 DiseaseOrPhenotypicFeature denotes VUR D014718

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T6 130-136 GeneOrGeneProduct denotes UP III
T17 145-148 DiseaseOrPhenotypicFeature denotes VUR D014718