PubMed:2793865 / 0-189 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"T1","span":{"begin":0,"end":106},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":106},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.\nA generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase ("}

    PubmedHPO

    {"project":"PubmedHPO","denotations":[{"id":"T1","span":{"begin":139,"end":152},"obj":"HP_0001427"}],"text":"Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.\nA generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase ("}

    DisGeNET5_gene_disease

    {"project":"DisGeNET5_gene_disease","denotations":[{"id":"2793865-0#43#79#gene4942","span":{"begin":43,"end":79},"obj":"gene4942"},{"id":"2793865-0#91#105#diseaseC0018425","span":{"begin":91,"end":105},"obj":"diseaseC0018425"}],"relations":[{"id":"43#79#gene494291#105#diseaseC0018425","pred":"associated_with","subj":"2793865-0#43#79#gene4942","obj":"2793865-0#91#105#diseaseC0018425"}],"text":"Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.\nA generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase ("}

    mondo_disease

    {"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":91,"end":105},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0009796"}],"text":"Point mutation affecting processing of the ornithine aminotransferase precursor protein in gyrate atrophy.\nA generalized deficiency of the mitochondrial enzyme, ornithine aminotransferase ("}