PubMed:2793865 / 0-231 JSONTXT

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{"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 (OAT) is the inborn error in gyrate atrophy"}

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{"project":"mondo_disease","denotations":[{"id":"T1","span":{"begin":91,"end":105},"obj":"Disease"},{"id":"T2","span":{"begin":189,"end":192},"obj":"Disease"},{"id":"T3","span":{"begin":217,"end":231},"obj":"Disease"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MONDO_0009796"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MONDO_0004483"},{"id":"A3","pred":"mondo_id","subj":"T3","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 (OAT) is the inborn error in gyrate atrophy"}