PubMed:2120217 / 0-71 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"T1","span":{"begin":0,"end":63},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":63},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Molecular basis of tyrosinase-negative oculocutaneous albinism. A singl"}

    DisGeNET

    {"project":"DisGeNET","denotations":[{"id":"T1","span":{"begin":19,"end":62},"obj":"disease:C0268494"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"Molecular basis of tyrosinase-negative oculocutaneous albinism. A singl"}

    DisGeNET5_variant_disease

    {"project":"DisGeNET5_variant_disease","denotations":[{"id":"2120217-0#39#62#diseaseC0078918","span":{"begin":39,"end":62},"obj":"diseaseC0078918"}],"text":"Molecular basis of tyrosinase-negative oculocutaneous albinism. A singl"}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"2120217-0#19#29#gene7299","span":{"begin":19,"end":29},"obj":"gene7299"},{"id":"2120217-0#39#62#diseaseC0078918","span":{"begin":39,"end":62},"obj":"diseaseC0078918"}],"relations":[{"id":"19#29#gene729939#62#diseaseC0078918","pred":"associated_with","subj":"2120217-0#19#29#gene7299","obj":"2120217-0#39#62#diseaseC0078918"}],"text":"Molecular basis of tyrosinase-negative oculocutaneous albinism. A singl"}

    PubCasesHPO

    {"project":"PubCasesHPO","denotations":[{"id":"TI1","span":{"begin":54,"end":62},"obj":"HP:0001022"}],"text":"Molecular basis of tyrosinase-negative oculocutaneous albinism. A singl"}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":19,"end":62},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0008745"}],"text":"Molecular basis of tyrosinase-negative oculocutaneous albinism. A singl"}

    HP-phenotype

    {"project":"HP-phenotype","denotations":[{"id":"T1","span":{"begin":54,"end":62},"obj":"Phenotype"}],"attributes":[{"id":"A1","pred":"hp_id","subj":"T1","obj":"HP:0001022"}],"namespaces":[{"prefix":"HP","uri":"http://purl.obolibrary.org/obo/HP_"}],"text":"Molecular basis of tyrosinase-negative oculocutaneous albinism. A singl"}