PubMed:15041272 / 1438-1564 JSONTXT

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TEST-DiseaseOrPhenotypicFeature

Id Subject Object Predicate Lexical cue #label
T8 41-44 DiseaseOrPhenotypicFeature denotes VWD D014842

Test-SequenceVariant

Id Subject Object Predicate Lexical cue
T4 84-90 SequenceVariant denotes R1306W

Test-GeneOrGeneProduct

Id Subject Object Predicate Lexical cue
T9 103-106 GeneOrGeneProduct denotes VWF

Test-merged-2

Id Subject Object Predicate Lexical cue #label
T57553 84-90 SequenceVariant denotes R1306W
T9 103-106 GeneOrGeneProduct denotes VWF
T8 41-44 DiseaseOrPhenotypicFeature denotes VWD D014842

Test-merged

Id Subject Object Predicate Lexical cue #label
T8 41-44 DiseaseOrPhenotypicFeature denotes VWD D014842
T9 103-106 GeneOrGeneProduct denotes VWF
T57553 84-90 SequenceVariant denotes R1306W

sentences

Id Subject Object Predicate Lexical cue
TextSentencer_T12 0-126 Sentence denotes In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described.
T12 0-126 Sentence denotes In conclusion, a first report of type 2B VWD in a Taiwanese Chinese family who show R1306W mutation in VWF gene was described.

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15041272-11#103#106#gene7450 103-106 gene7450 denotes VWF
15041272-11#41#44#diseaseC1282971 41-44 diseaseC1282971 denotes VWD
103#106#gene745041#44#diseaseC1282971 15041272-11#103#106#gene7450 15041272-11#41#44#diseaseC1282971 associated_with VWF,VWD

tmVarCorpus

Id Subject Object Predicate Lexical cue
T4 84-90 ProteinMutation:p|SUB|R|1306|W denotes R1306W

DisGeNET

Id Subject Object Predicate Lexical cue
T0 103-106 gene:7450 denotes VWF
T1 41-44 disease:C1282971 denotes VWD
R1 T0 T1 associated_with VWF,VWD