PubMed:2120217 / 19-62
Annnotations
DisGeNET
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-43 | disease:C0268494 | denotes | tyrosinase-negative oculocutaneous albinism |
DisGeNET5_variant_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
2120217-0#39#62#diseaseC0078918 | 20-43 | diseaseC0078918 | denotes | oculocutaneous albinism |
DisGeNET5_gene_disease
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
2120217-0#19#29#gene7299 | 0-10 | gene7299 | denotes | tyrosinase |
2120217-0#39#62#diseaseC0078918 | 20-43 | diseaseC0078918 | denotes | oculocutaneous albinism |
19#29#gene729939#62#diseaseC0078918 | 2120217-0#19#29#gene7299 | 2120217-0#39#62#diseaseC0078918 | associated_with | tyrosinase,oculocutaneous albinism |
PubCasesHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
TI1 | 35-43 | HP:0001022 | denotes | albinism |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 0-43 | Disease | denotes | tyrosinase-negative oculocutaneous albinism | http://purl.obolibrary.org/obo/MONDO_0008745 |
HP-phenotype
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T1 | 35-43 | Phenotype | denotes | albinism | HP:0001022 |