PubMed:10102532 / 0-73 JSONTXT

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    PMID_GLOBAL

    {"project":"PMID_GLOBAL","denotations":[{"id":"T1","span":{"begin":0,"end":22},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0019565"},{"id":"A2","pred":"mondo_id","subj":"T1","obj":"0024574"}],"text":"von Willebrand disease with G4022A mutation (vWd Sungnam): a case report."}

    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":73},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":73},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"von Willebrand disease with G4022A mutation (vWd Sungnam): a case report."}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":0,"end":22},"obj":"ORDO:903"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"von Willebrand disease with G4022A mutation (vWd Sungnam): a case report."}