PubMed:21219851 / 248-275
Annnotations
LitCoin-entities
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
8485 | 0-27 | DiseaseOrPhenotypicFeature | denotes | autosomal dominant disorder | MESH:D030342 |
LitCoin-Disease-MeSH
Id | Subject | Object | Predicate | Lexical cue | originalLabel |
---|---|---|---|---|---|
T3 | 0-27 | DiseaseOrPhenotypicFeature | denotes | autosomal dominant disorder | DISEASE |
LitCoin-MeSH-Disease-2
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T5 | 0-27 | DiseaseOrPhenotypicFeature | denotes | autosomal dominant disorder | DISEASE |
LitCoin-MONDO_bioort2019
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T5 | 0-27 | DiseaseOrPhenotypicFeature | denotes | autosomal dominant disorder | DISEASE |
LitCoin-training-merged
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T32104 | 0-27 | DiseaseOrPhenotypicFeature | denotes | autosomal dominant disorder | DISEASE |
PubmedHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-18 | HP_0000006 | denotes | autosomal dominant |