@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:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_head { this: np:hasAssertion dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_assertion; np:hasProvenance dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_provenance; np:hasPublicationInfo dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_publicationInfo; a np:Nanopublication . dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_assertion a np:Assertion . dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_provenance a np:Provenance . dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_publicationInfo a np:PublicationInfo . } dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_assertion { miriam-gene:1535 a ncit:C16612 . lld:C0003850 a ncit:C7057 . dgn-gda:DGNaa47110e61086c1424343df625c0be6b sio:SIO_000628 miriam-gene:1535, lld:C0003850; a sio:SIO_001121 . } dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_provenance { dgn-np:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_assertion dcterms:description "[Although polymorphisms of the P22PHOX gene located in the coding region and the 3'-untranslated region were reported to be associated with atherosclerosis and cerebrovascular disease, our data provide evidence that there is no association between these polymorphisms and the occurrence of cerebral aneurysms in Caucasians.]. 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:13130177; 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:NP338654.RAGd6HtD3H_55EPdQun-HdzTKmCkVTE8CkkKEy_a3bG9o130_publicationInfo { this: dcterms:created "2015-08-25T14:40:55+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" . }