PubMed:15041272 / 0-135 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/15041272","sourcedb":"PubMed","sourceid":"15041272","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/15041272","text":"A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation.\nClinical, laboratory and genetic defect of a T","tracks":[{"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"},{"subj":"T1","pred":"source","obj":"TEST-DiseaseOrPhenotypicFeature"},{"subj":"T2","pred":"source","obj":"TEST-DiseaseOrPhenotypicFeature"}]},{"project":"Test-SequenceVariant","denotations":[{"id":"T1","span":{"begin":72,"end":78},"obj":"SequenceVariant"}],"attributes":[{"subj":"T1","pred":"source","obj":"Test-SequenceVariant"}]},{"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"},{"subj":"T46254","pred":"source","obj":"Test-merged-2"},{"subj":"T1","pred":"source","obj":"Test-merged-2"},{"subj":"T2","pred":"source","obj":"Test-merged-2"}]},{"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"},{"subj":"T2","pred":"source","obj":"Test-merged"},{"subj":"T1","pred":"source","obj":"Test-merged"},{"subj":"T46254","pred":"source","obj":"Test-merged"}]},{"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#"}],"attributes":[{"subj":"TextSentencer_T1","pred":"source","obj":"sentences"},{"subj":"T1","pred":"source","obj":"sentences"}]},{"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"}],"attributes":[{"subj":"15041272-0#72#78#geners61749384","pred":"source","obj":"DisGeNET5_variant_disease"},{"subj":"15041272-0#36#66#diseaseC1282971","pred":"source","obj":"DisGeNET5_variant_disease"}]},{"project":"PubCasesORDO","denotations":[{"id":"TI1","span":{"begin":44,"end":66},"obj":"ORDO:903"}],"namespaces":[{"prefix":"ORDO","uri":"http://www.orpha.net/ORDO/Orphanet_"}],"attributes":[{"subj":"TI1","pred":"source","obj":"PubCasesORDO"}]},{"project":"tmVarCorpus","denotations":[{"id":"T1","span":{"begin":72,"end":78},"obj":"ProteinMutation:p|SUB|R|1306|W"}],"attributes":[{"subj":"T1","pred":"source","obj":"tmVarCorpus"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"TEST-DiseaseOrPhenotypicFeature","color":"#ecb893","default":true},{"id":"Test-SequenceVariant","color":"#9e93ec"},{"id":"Test-merged-2","color":"#a2ec93"},{"id":"Test-merged","color":"#ec93bc"},{"id":"sentences","color":"#93d6ec"},{"id":"DisGeNET5_variant_disease","color":"#ece893"},{"id":"PubCasesORDO","color":"#ce93ec"},{"id":"tmVarCorpus","color":"#93ecb4"}]}]}}