@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_head { this: np:hasAssertion dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_assertion; np:hasProvenance dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_provenance; np:hasPublicationInfo dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_publicationInfo; a np:Nanopublication . dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_assertion a np:Assertion . dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_provenance a np:Provenance . dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_publicationInfo a np:PublicationInfo . } dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_assertion { miriam-gene:7450 a ncit:C16612 . lld:C0042974 a ncit:C7057 . dgn-gda:DGNbfcaa7d0c247b81330e2fd410c21a002 sio:SIO_000628 miriam-gene:7450, lld:C0042974; a sio:SIO_001121 . } dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_provenance { dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_assertion dcterms:description "[Two unrelated families were recruited in the French Reference Center for von Willebrand Disease with moderate bleeding symptoms associated with low von Willebrand factor (VWF) antigen levels, decreased collagen binding assay, and no or partial response to desmopressin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:23335371; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1045430.RA93F_f964S8IdZvgXgMGVM1McnGHWVJNbdFxB7NhK_8U130_publicationInfo { this: dcterms:created "2016-05-13T12:49:40+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }