PubMed:15041272 / 89-206 JSONTXT

Annnotations TAB JSON ListView MergeView

    TEST-DiseaseOrPhenotypicFeature

    {"project":"TEST-DiseaseOrPhenotypicFeature","denotations":[{"id":"T2","span":{"begin":25,"end":39},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":67,"end":97},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":99,"end":102},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"DISEASE"},{"id":"A3","pred":"#label","subj":"T3","obj":"D056728"},{"id":"A4","pred":"#label","subj":"T4","obj":"D014842"}],"text":"Clinical, laboratory and genetic defect of a Taiwanese family with type 2B von Willebrand disease (VWD) were studied."}

    Test-merged-2

    {"project":"Test-merged-2","denotations":[{"id":"T2","span":{"begin":25,"end":39},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":67,"end":97},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":99,"end":102},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"DISEASE"},{"id":"A3","pred":"#label","subj":"T3","obj":"D056728"},{"id":"A4","pred":"#label","subj":"T4","obj":"D014842"}],"text":"Clinical, laboratory and genetic defect of a Taiwanese family with type 2B von Willebrand disease (VWD) were studied."}

    Test-merged

    {"project":"Test-merged","denotations":[{"id":"T4","span":{"begin":99,"end":102},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":67,"end":97},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":25,"end":39},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A4","pred":"#label","subj":"T4","obj":"D014842"},{"id":"A3","pred":"#label","subj":"T3","obj":"D056728"},{"id":"A2","pred":"#label","subj":"T2","obj":"DISEASE"}],"text":"Clinical, laboratory and genetic defect of a Taiwanese family with type 2B von Willebrand disease (VWD) were studied."}

    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":117},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":117},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Clinical, laboratory and genetic defect of a Taiwanese family with type 2B von Willebrand disease (VWD) were studied."}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"AB1","span":{"begin":75,"end":97},"obj":"ORDO:903"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"Clinical, laboratory and genetic defect of a Taiwanese family with type 2B von Willebrand disease (VWD) were studied."}