@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:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_head { this: np:hasAssertion dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_assertion; np:hasProvenance dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_provenance; np:hasPublicationInfo dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_publicationInfo; a np:Nanopublication . dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_assertion a np:Assertion . dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_provenance a np:Provenance . dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_publicationInfo a np:PublicationInfo . } dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_assertion { miriam-gene:348 a ncit:C16612 . lld:C2748208 a ncit:C7057 . dgn-gda:DGNac75027629f07ab946f0eff45b77ed31 sio:SIO_000628 miriam-gene:348, lld:C2748208; a sio:SIO_001121 . } dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_provenance { dgn-np:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_assertion dcterms:description "[The findings suggest that patients with brain tumors who are carriers of the APOE ε4 allele may have increased vulnerability to developing memory and executive dysfunction, and that additional SNPs in the APOE gene may be associated with cognitive outcome.]. 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:24944262; 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:NP246574.RAoP3JZ7-pL1SNjleSyC-vOwfUaCEass7lFM47wa3kEms130_publicationInfo { this: dcterms:created "2015-08-25T14:40:00+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" . }