@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:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_head { this: np:hasAssertion dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_assertion; np:hasProvenance dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_provenance; np:hasPublicationInfo dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_publicationInfo; a np:Nanopublication . dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_assertion a np:Assertion . dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_provenance a np:Provenance . dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_publicationInfo a np:PublicationInfo . } dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_assertion { miriam-gene:3557 a ncit:C16612 . lld:C3494652 a ncit:C7057 . dgn-gda:DGN5c6f5e75fecd8d0d289436186392cfc9 sio:SIO_000628 miriam-gene:3557, lld:C3494652; a sio:SIO_001121 . } dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_provenance { dgn-np:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_assertion dcterms:description "[IL-1A TT and IL-1B CT/TT associated genotypes were at risk of Alzheimer's disease (odds ratio 4.80 (95% confidence interval, 1.32 to 17.40), p = 0.017); the MTR 2756 AA genotype was at risk of severe dementia (OR 2.97 (1.23 to 7.21), p = 0.016); IL-1 RN*2 was protective (OR 0.28, (0.11 to 0.69), p = 0.006).]. 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:15201366; 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:NP491880.RAgHrHFBxWKxHyVKKAhH--tYCnKbuzqsuthpAvtEqhbKU130_publicationInfo { this: dcterms:created "2015-08-25T14:42:30+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" . }