> top > docs > PubMed:2120217 > spans > 19-62 > annotations

PubMed:2120217 / 19-62 JSONTXT

Annnotations TAB JSON ListView MergeView

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