PubMed:26900322 / 219-372
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 11068 | 87-90 | GeneOrGeneProduct | denotes | CFI | NCBIGene:3426 |
| 11069 | 117-152 | DiseaseOrPhenotypicFeature | denotes | Vogt-Koyanagi-Harada (VKH) syndrome | MESH:D014607 |
LitCoin-sentences
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T4 | 0-153 | Sentence | denotes | The present study was performed to investigate the existence of an association between CFI genetic polymorphisms and Vogt-Koyanagi-Harada (VKH) syndrome. |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T4 | 144-152 | GeneOrGeneProduct | denotes | syndrome |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T3 | 144-152 | GeneOrGeneProduct | denotes | syndrome |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T3 | 138-152 | DiseaseOrPhenotypicFeature | denotes | (VKH) syndrome | D014607 |
LitCoin-GeneOrGeneProduct-v3
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T4 | 87-90 | GeneOrGeneProduct | denotes | CFI |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T3 | 138-152 | DiseaseOrPhenotypicFeature | denotes | (VKH) syndrome | 0018092 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T3 | 117-152 | DiseaseOrPhenotypicFeature | denotes | Vogt-Koyanagi-Harada (VKH) syndrome | DISEASE |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T3 | 117-152 | DiseaseOrPhenotypicFeature | denotes | Vogt-Koyanagi-Harada (VKH) syndrome | DISEASE |
LitCoin-Chemical-MeSH-CHEBI
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T3 | 87-90 | ChemicalEntity | denotes | CFI | C010073 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label | ID: |
|---|---|---|---|---|---|---|
| T3 | 87-90 | ChemicalEntity | denotes | CFI | C010073 | |
| T84934 | 87-90 | GeneOrGeneProduct | denotes | CFI | ||
| T42418 | 117-152 | DiseaseOrPhenotypicFeature | denotes | Vogt-Koyanagi-Harada (VKH) syndrome | DISEASE |