> top > docs > PubMed:24477591 > spans > 966-1060 > annotations

PubMed:24477591 / 966-1060 JSONTXT

Annnotations TAB JSON ListView MergeView

LitCoin-sentences

Id Subject Object Predicate Lexical cue
T10 0-94 Sentence denotes The -930G allele carrier state was a risk factor for CAD (OR 2.03, 95% CI 1.21-3.44, P=0.007).

LitCoin-entities

Id Subject Object Predicate Lexical cue db_id
9613 4-9 SequenceVariant denotes -930G DBSNP:rs9932581
9614 53-56 DiseaseOrPhenotypicFeature denotes CAD MESH:D003324

LitCoin-SeqVar

Id Subject Object Predicate Lexical cue
T6 5-9 SequenceVariant denotes 930G

LitCoin-GeneOrGeneProduct-v2

Id Subject Object Predicate Lexical cue
T12 17-24 GeneOrGeneProduct denotes carrier
T13 42-48 GeneOrGeneProduct denotes factor

LitCoin-GeneOrGeneProduct-v0

Id Subject Object Predicate Lexical cue
T20 17-24 GeneOrGeneProduct denotes carrier
T21 42-48 GeneOrGeneProduct denotes factor

LitCoin-Disease-MeSH

Id Subject Object Predicate Lexical cue originalLabel
T7 53-56 DiseaseOrPhenotypicFeature denotes CAD D003324

LitCoin_Mondo_095

Id Subject Object Predicate Lexical cue mondo_id
T13 53-56 DiseaseOrPhenotypicFeature denotes CAD 0100077|0018922|0005010

LitCoin-MeSH-Disease-2

Id Subject Object Predicate Lexical cue ID:
T7 53-56 DiseaseOrPhenotypicFeature denotes CAD D003324

LitCoin-MONDO_bioort2019

Id Subject Object Predicate Lexical cue #label
T7 53-56 DiseaseOrPhenotypicFeature denotes CAD D003324

LitCoin-training-merged

Id Subject Object Predicate Lexical cue #label
T93894 53-56 DiseaseOrPhenotypicFeature denotes CAD D003324
T9852 5-9 SequenceVariant denotes 930G