@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:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_head { this: np:hasAssertion dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_assertion; np:hasProvenance dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_provenance; np:hasPublicationInfo dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_publicationInfo; a np:Nanopublication . dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_assertion a np:Assertion . dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_provenance a np:Provenance . dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_publicationInfo a np:PublicationInfo . } dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_assertion { miriam-gene:5277 a ncit:C16612 . lld:C0024790 a ncit:C7057 . dgn-gda:DGN25a3509f53113a03c32d9740a9e72aea sio:SIO_000628 miriam-gene:5277, lld:C0024790; a sio:SIO_001121 . } dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_provenance { dgn-np:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_assertion dcterms:description "[CD59 deficiency is a common finding in RBCs and WBCs in patients with chronic hemolysis suffering from paroxysmal nocturnal hemoglobinuria in which the acquired mutation in the PIGA gene leads to membrane loss of glycosylphosphatidylinositol-anchored membrane proteins, including CD59.]. 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:23149847; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP620568.RA9BW_l1M3Xkww9oGXl3aUBLkbJ7vgoRA459sDW4Wet7k130_publicationInfo { this: dcterms:created "2015-08-25T14:43:51+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }