PubMed:15041272 / 0-135 JSONTXT

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    TEST-DiseaseOrPhenotypicFeature

    {"project":"TEST-DiseaseOrPhenotypicFeature","denotations":[{"id":"T1","span":{"begin":36,"end":66},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":114,"end":128},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D056728"},{"id":"A2","pred":"#label","subj":"T2","obj":"DISEASE"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}

    Test-SequenceVariant

    {"project":"Test-SequenceVariant","denotations":[{"id":"T1","span":{"begin":72,"end":78},"obj":"SequenceVariant"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}

    Test-merged-2

    {"project":"Test-merged-2","denotations":[{"id":"T46254","span":{"begin":72,"end":78},"obj":"SequenceVariant"},{"id":"T1","span":{"begin":36,"end":66},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":114,"end":128},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"D056728"},{"id":"A2","pred":"#label","subj":"T2","obj":"DISEASE"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}

    Test-merged

    {"project":"Test-merged","denotations":[{"id":"T2","span":{"begin":114,"end":128},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T1","span":{"begin":36,"end":66},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T46254","span":{"begin":72,"end":78},"obj":"SequenceVariant"}],"attributes":[{"id":"A2","pred":"#label","subj":"T2","obj":"DISEASE"},{"id":"A1","pred":"#label","subj":"T1","obj":"D056728"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}

    sentences

    {"project":"sentences","denotations":[{"id":"TextSentencer_T1","span":{"begin":0,"end":88},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":88},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}

    DisGeNET5_variant_disease

    {"project":"DisGeNET5_variant_disease","denotations":[{"id":"15041272-0#72#78#geners61749384","span":{"begin":72,"end":78},"obj":"geners61749384"},{"id":"15041272-0#36#66#diseaseC1282971","span":{"begin":36,"end":66},"obj":"diseaseC1282971"}],"relations":[{"id":"72#78#geners6174938436#66#diseaseC1282971","pred":"associated_with","subj":"15041272-0#72#78#geners61749384","obj":"15041272-0#36#66#diseaseC1282971"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}

    PubCasesORDO

    {"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":44,"end":66},"obj":"ORDO:903"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}

    tmVarCorpus

    {"project":"tmVarCorpus","denotations":[{"id":"T1","span":{"begin":72,"end":78},"obj":"ProteinMutation:p|SUB|R|1306|W"}],"text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T"}