@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:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_head { this: np:hasAssertion dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_assertion; np:hasProvenance dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_provenance; np:hasPublicationInfo dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_publicationInfo; a np:Nanopublication . dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_assertion a np:Assertion . dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_provenance a np:Provenance . dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_publicationInfo a np:PublicationInfo . } dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_assertion { miriam-gene:966 a ncit:C16612 . lld:C2676767 a ncit:C7057 . dgn-gda:DGNda92c5124e11e86beb8d989086a489f3 sio:SIO_000628 miriam-gene:966, lld:C2676767; a sio:SIO_001122 . } dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_provenance { dgn-np:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_assertion dcterms:description "[In this review we describe differences and similarities in the pathogenesis and clinical manifestations of PNH and primary CD59 Cys89Tyr mutation with the aim of tracking the contribution of CD59 deficiency to the pathophysiology and perhaps deepening our understanding of both diseases.]. 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:25818314; 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:NP1274489.RA8RIohSp4Sr0gTY9RGz0XDwovBgmTU8Tnft2DFBx1ujg130_publicationInfo { this: dcterms:created "2016-05-13T12:51:24+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" . }