@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:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_head { this: np:hasAssertion dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_assertion; np:hasProvenance dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_provenance; np:hasPublicationInfo dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_publicationInfo; a np:Nanopublication . dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_assertion a np:Assertion . dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_provenance a np:Provenance . dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_publicationInfo a np:PublicationInfo . } dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_assertion { miriam-gene:348 a ncit:C16612 . lld:C0014544 a ncit:C7057 . dgn-gda:DGNd443eac435786f3313aac053c1939d1a sio:SIO_000628 miriam-gene:348, lld:C0014544; a sio:SIO_001121 . } dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_provenance { dgn-np:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_assertion dcterms:description "[Our findings of neuronal and glial events, which correlate with lesser neuronal DNA damage and larger, more robust neurons in epilepsy patients of APOE ε3,3 genotype compared to APOE ε4,4 genotype carriers, are consistent with the idea that the APOE ε3,3 genotype better protects neurons subjected to the hyperexcitability of epilepsy and thus confers less risk of AD (Alzheimer's disease).Please see related article: http://www.biomedcentral.com/1741-7015/10/36.]. 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:22502727; 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:NP974742.RA1pObYQNPHdD1PkM06teOv15ob044pvu2uaj8I_Yft-8130_publicationInfo { this: dcterms:created "2016-05-13T12:49:06+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" . }