PubMed:26581643 / 169-328 JSONTXT

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{"project":"sentences","denotations":[{"id":"T3","span":{"begin":0,"end":159},"obj":"Sentence"},{"id":"T3","span":{"begin":0,"end":159},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Huntington's disease (HD) is an autosomal dominant disorder of central nervous system caused by expansion of CAG repeats in exon1 of the huntingtin gene (Htt)."}

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{"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":63,"end":85},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/UBERON_0001017"}],"text":"Huntington's disease (HD) is an autosomal dominant disorder of central nervous system caused by expansion of CAG repeats in exon1 of the huntingtin gene (Htt)."}

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