PubMed:1906877 / 1222-1413
Annnotations
sentences
{"project":"sentences","denotations":[{"id":"TextSentencer_T12","span":{"begin":0,"end":191},"obj":"Sentence"},{"id":"T12","span":{"begin":0,"end":191},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"These observations suggest a critical role for Arg91 in the interaction of vWF with FVIII and identify the molecular mechanism for a variant of vWD associated with unusually low FVIII levels."}
DisGeNET
{"project":"DisGeNET","denotations":[{"id":"T0","span":{"begin":75,"end":78},"obj":"gene:7450"},{"id":"T1","span":{"begin":144,"end":147},"obj":"disease:C0042974"}],"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":"These observations suggest a critical role for Arg91 in the interaction of vWF with FVIII and identify the molecular mechanism for a variant of vWD associated with unusually low FVIII levels."}
DisGeNET5_gene_disease
{"project":"DisGeNET5_gene_disease","denotations":[{"id":"1906877-6#75#78#gene7450","span":{"begin":75,"end":78},"obj":"gene7450"},{"id":"1906877-6#144#147#diseaseC0042974","span":{"begin":144,"end":147},"obj":"diseaseC0042974"}],"relations":[{"id":"75#78#gene7450144#147#diseaseC0042974","pred":"associated_with","subj":"1906877-6#75#78#gene7450","obj":"1906877-6#144#147#diseaseC0042974"}],"text":"These observations suggest a critical role for Arg91 in the interaction of vWF with FVIII and identify the molecular mechanism for a variant of vWD associated with unusually low FVIII levels."}
mondo_disease
{"project":"mondo_disease","denotations":[{"id":"T6","span":{"begin":144,"end":147},"obj":"Disease"}],"attributes":[{"id":"A6","pred":"mondo_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/MONDO_0019565"}],"text":"These observations suggest a critical role for Arg91 in the interaction of vWF with FVIII and identify the molecular mechanism for a variant of vWD associated with unusually low FVIII levels."}