PubMed:18470323 / 25-57
Annnotations
LitCoin-entities
| Id | Subject | Object | Predicate | Lexical cue | db_id |
|---|---|---|---|---|---|
| 5076 | 0-32 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | MESH:C537881 |
LitCoin_Mondo
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 0-32 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | 0007380 |
| T2 | 0-25 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy | 0004686 |
| T3 | 8-25 | DiseaseOrPhenotypicFeature | denotes | corneal dystrophy | 0018102 |
LitCoin-GeneOrGeneProduct-v2
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 26-32 | GeneOrGeneProduct | denotes | type I |
LitCoin-GeneOrGeneProduct-v0
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 26-32 | GeneOrGeneProduct | denotes | type I |
LitCoin-Disease-MeSH
| Id | Subject | Object | Predicate | Lexical cue | originalLabel |
|---|---|---|---|---|---|
| T1 | 8-25 | DiseaseOrPhenotypicFeature | denotes | corneal dystrophy | D003317 |
LitCoin_Mondo_095
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 0-32 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | 0007380 |
PMID_GLOBAL
| Id | Subject | Object | Predicate | Lexical cue | mondo_id |
|---|---|---|---|---|---|
| T1 | 0-32 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | 0007380 |
LitCoin-MeSH-Disease-2
| Id | Subject | Object | Predicate | Lexical cue | ID: |
|---|---|---|---|---|---|
| T1 | 8-25 | DiseaseOrPhenotypicFeature | denotes | corneal dystrophy | D003317 |
LitCoin-MONDO_bioort2019
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T1 | 0-32 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | C537881 |
LitCoin-training-merged
| Id | Subject | Object | Predicate | Lexical cue | #label |
|---|---|---|---|---|---|
| T50708 | 0-32 | DiseaseOrPhenotypicFeature | denotes | lattice corneal dystrophy type I | C537881 |
DisGeNET
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| T1 | 0-32 | disease:C1690006 | denotes | lattice corneal dystrophy type I |
| T3 | 0-32 | disease:C1690006 | denotes | lattice corneal dystrophy type I |
DisGeNET5_variant_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 18470323-0#25#57#diseaseC1690006 | 0-32 | diseaseC1690006 | denotes | lattice corneal dystrophy type I |
DisGeNET5_gene_disease
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| 18470323-0#25#57#diseaseC1690006 | 0-32 | diseaseC1690006 | denotes | lattice corneal dystrophy type I |
PubCasesHPO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TI1 | 0-25 | HP:0001149 | denotes | lattice corneal dystrophy |
PubCasesORDO
| Id | Subject | Object | Predicate | Lexical cue |
|---|---|---|---|---|
| TI1 | 0-32 | ORDO:98964 | denotes | lattice corneal dystrophy type I |