PubMed:16440883 / 781-934 JSONTXT

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    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T9","span":{"begin":0,"end":153},"obj":"Sentence"},{"id":"T9","span":{"begin":0,"end":153},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Only eight patients with Apert syndrome and preaxial polydactyly have been reported and this is the first case in which molecular diagnosis is available."}

    PubmedHPO

    {"project":"PubmedHPO","denotations":[{"id":"T13","span":{"begin":44,"end":64},"obj":"HP_0100258"},{"id":"T14","span":{"begin":53,"end":64},"obj":"HP_0010442"}],"text":"Only eight patients with Apert syndrome and preaxial polydactyly have been reported and this is the first case in which molecular diagnosis is available."}

    PubCasesHPO

    {"project":"PubCasesHPO","denotations":[{"id":"AB7","span":{"begin":44,"end":64},"obj":"HP:0100258"}],"text":"Only eight patients with Apert syndrome and preaxial polydactyly have been reported and this is the first case in which molecular diagnosis is available."}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"AB4","span":{"begin":25,"end":39},"obj":"ORDO:87"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Only eight patients with Apert syndrome and preaxial polydactyly have been reported and this is the first case in which molecular diagnosis is available."}