@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:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_head { this: np:hasAssertion dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_assertion; np:hasProvenance dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_provenance; np:hasPublicationInfo dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_publicationInfo; a np:Nanopublication . dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_assertion a np:Assertion . dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_provenance a np:Provenance . dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_publicationInfo a np:PublicationInfo . } dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_assertion { miriam-gene:7450 a ncit:C16612 . lld:C1264041 a ncit:C7057 . dgn-gda:DGNc36df13d5991fcd2718688d1716258f5 sio:SIO_000628 miriam-gene:7450, lld:C1264041; a sio:SIO_001121 . } dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_provenance { dgn-np:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_assertion dcterms:description "[The detection of even tiny amounts of von Willebrand factor (VWF):antigen after desmopressin treatment or in hidden sites like platelets allows the differentiation between patients with recessive von Willebrand disease (VWD) type 3, severe type 1, and 2C (2A subtype IIC).]. 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:19506357; 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:NP743882.RA1ae-TBCjbdRT6f2C8pDyikCKqi46-lLY4uyObar90Jk130_publicationInfo { this: dcterms:created "2016-05-13T12:47:22+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" . }