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PubMed:19057677 JSONTXT

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PMID_GLOBAL

Id Subject Object Predicate Lexical cue mondo_id
T1 159-163 DiseaseOrPhenotypicFeature denotes skin 0002531
T2 361-375 DiseaseOrPhenotypicFeature denotes skin disorders 0005093
T3 389-397 DiseaseOrPhenotypicFeature denotes vitiligo 0008661|0011684
T5 400-420 DiseaseOrPhenotypicFeature denotes neurologic disorders 0005071
T6 422-441 DiseaseOrPhenotypicFeature denotes Parkinson's disease 0005180
T7 464-486 DiseaseOrPhenotypicFeature denotes Waardenburg's syndrome 0018094
T8 518-550 DiseaseOrPhenotypicFeature denotes age related macular degeneration 0005150
T9 1651-1659 DiseaseOrPhenotypicFeature denotes melanoma 0005105

DisGeNET

Id Subject Object Predicate Lexical cue
T0 1616-1626 gene:7299 denotes tyrosinase
T1 1651-1659 disease:C0025202 denotes melanoma
R1 T0 T1 associated_with tyrosinase,melanoma

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
19057677-8#102#112#gene7299 1616-1626 gene7299 denotes tyrosinase
19057677-8#137#145#diseaseC0025202 1651-1659 diseaseC0025202 denotes melanoma
102#112#gene7299137#145#diseaseC0025202 19057677-8#102#112#gene7299 19057677-8#137#145#diseaseC0025202 associated_with tyrosinase,melanoma