PubMed:7668252 / 862-878
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 126 | 0-16 | DiseaseOrPhenotypicFeature | denotes | VLCAD deficiency | MESH:C536353 |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T32 | 0-5 | GeneOrGeneProduct | denotes | VLCAD |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T23 | 0-5 | GeneOrGeneProduct | denotes | VLCAD |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T2 | 0-16 | DiseaseOrPhenotypicFeature | denotes | VLCAD deficiency | C536353 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T6 | 0-16 | DiseaseOrPhenotypicFeature | denotes | VLCAD deficiency | 0008723 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T1 | 0-16 | DiseaseOrPhenotypicFeature | denotes | VLCAD deficiency | C536353 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T2 | 0-16 | DiseaseOrPhenotypicFeature | denotes | VLCAD deficiency | C536353 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T50975 | 0-16 | DiseaseOrPhenotypicFeature | denotes | VLCAD deficiency | C536353 |
NCBIDiseaseCorpus
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-16 | SpecificDisease:C536353 | denotes | VLCAD deficiency |
testtesttest
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T2 | 0-16 | SpecificDisease:C536353 | denotes | VLCAD deficiency |
NCBI-Disease-Train
| Id | Subject | Object | Predicate | Lexical cue | database_id |
|---|---|---|---|---|---|
| T2996 | 0-16 | SpecificDisease | denotes | VLCAD deficiency | C536353 |