PubMed:24477591 / 966-1060
Annnotations
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 |