PubMed:15041272 / 1438-1564 JSONTXT

{"project":"TEST-DiseaseOrPhenotypicFeature","denotations":[{"id":"T8","span":{"begin":41,"end":44},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"#label","subj":"T8","obj":"D014842"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"Test-SequenceVariant","denotations":[{"id":"T4","span":{"begin":84,"end":90},"obj":"SequenceVariant"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"Test-GeneOrGeneProduct","denotations":[{"id":"T9","span":{"begin":103,"end":106},"obj":"GeneOrGeneProduct"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"Test-merged-2","denotations":[{"id":"T57553","span":{"begin":84,"end":90},"obj":"SequenceVariant"},{"id":"T9","span":{"begin":103,"end":106},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":41,"end":44},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A8","pred":"#label","subj":"T8","obj":"D014842"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"Test-merged","denotations":[{"id":"T8","span":{"begin":41,"end":44},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T9","span":{"begin":103,"end":106},"obj":"GeneOrGeneProduct"},{"id":"T57553","span":{"begin":84,"end":90},"obj":"SequenceVariant"}],"attributes":[{"id":"A8","pred":"#label","subj":"T8","obj":"D014842"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"sentences","denotations":[{"id":"TextSentencer_T12","span":{"begin":0,"end":126},"obj":"Sentence"},{"id":"T12","span":{"begin":0,"end":126},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"DisGeNET5_gene_disease","denotations":[{"id":"15041272-11#103#106#gene7450","span":{"begin":103,"end":106},"obj":"gene7450"},{"id":"15041272-11#41#44#diseaseC1282971","span":{"begin":41,"end":44},"obj":"diseaseC1282971"}],"relations":[{"id":"103#106#gene745041#44#diseaseC1282971","pred":"associated_with","subj":"15041272-11#103#106#gene7450","obj":"15041272-11#41#44#diseaseC1282971"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"tmVarCorpus","denotations":[{"id":"T4","span":{"begin":84,"end":90},"obj":"ProteinMutation:p|SUB|R|1306|W"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}

{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":103,"end":106},"obj":"gene:7450"},{"id":"T1","span":{"begin":41,"end":44},"obj":"disease:C1282971"}],"relations":[{"id":"R1","pred":"associated_with","subj":"T0","obj":"T1"}],"namespaces":[{"prefix":"gene","uri":"http://www.ncbi.nlm.nih.gov/gene/"},{"prefix":"disease","uri":"http://purl.bioontology.org/ontology/MEDLINEPLUS/"}],"text":"In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described."}