@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:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_head { this: np:hasAssertion dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_assertion; np:hasProvenance dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_provenance; np:hasPublicationInfo dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_publicationInfo; a np:Nanopublication . dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_assertion a np:Assertion . dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_provenance a np:Provenance . dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_publicationInfo a np:PublicationInfo . } dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_assertion { miriam-gene:7450 a ncit:C16612 . lld:C0042974 a ncit:C7057 . dgn-gda:DGN6e716fe07e0db0df3d68f90735425625 sio:SIO_000628 miriam-gene:7450, lld:C0042974; a sio:SIO_001121 . } dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_provenance { dgn-np:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_assertion dcterms:description "[We have identified a patient with von Willebrand's disease (vWD) resembling type IIB vWD, with increased ristocetin induced platelet aggregation (RIPA), the absence of the large multimers of von Willebrand factor (vWF) in plasma, and the presence of the large multimers in platelets in whom a family study indicated a probable double heterozygous inheritance pattern.]. 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:1609773; 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:NP508593.RA_JyUuc7bJjpujRDvkaVIiXbEZ8xHxj401AkZLVRQi5s130_publicationInfo { this: dcterms:created "2016-05-13T12:45:35+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" . }