PubMed:20846357 / 611-623
Annnotations
LitCoin-entities
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
8062 | 0-12 | DiseaseOrPhenotypicFeature | denotes | KID syndrome | MESH:C536168 |
LitCoin_Mondo
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T9 | 0-12 | DiseaseOrPhenotypicFeature | denotes | KID syndrome | 0018781 |
LitCoin-GeneOrGeneProduct-v0
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T22 | 4-12 | GeneOrGeneProduct | denotes | syndrome |
LitCoin-GeneOrGeneProduct-v2
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T13 | 4-12 | GeneOrGeneProduct | denotes | syndrome |
LitCoin-Disease-MeSH
Id | Subject | Object | Predicate | Lexical cue | originalLabel |
---|---|---|---|---|---|
T3 | 0-12 | DiseaseOrPhenotypicFeature | denotes | KID syndrome | C536168 |
LitCoin_Mondo_095
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T4 | 0-12 | DiseaseOrPhenotypicFeature | denotes | KID syndrome | 0018781 |
LitCoin-MeSH-Disease-2
Id | Subject | Object | Predicate | Lexical cue | ID: |
---|---|---|---|---|---|
T4 | 0-12 | DiseaseOrPhenotypicFeature | denotes | KID syndrome | C536168 |
LitCoin-MONDO_bioort2019
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T4 | 0-12 | DiseaseOrPhenotypicFeature | denotes | KID syndrome | C536168 |
LitCoin-training-merged
Id | Subject | Object | Predicate | Lexical cue | #label |
---|---|---|---|---|---|
T59486 | 0-12 | DiseaseOrPhenotypicFeature | denotes | KID syndrome | C536168 |
PubCasesORDO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
AB2 | 0-12 | ORDO:477 | denotes | KID syndrome |