@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:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_head { this: np:hasAssertion dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_assertion; np:hasProvenance dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_provenance; np:hasPublicationInfo dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_publicationInfo; a np:Nanopublication . dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_assertion a np:Assertion . dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_provenance a np:Provenance . dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_publicationInfo a np:PublicationInfo . } dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_assertion { miriam-gene:27286 a ncit:C16612 . lld:C0014544 a ncit:C7057 . dgn-gda:DGN9570ee3f9eba7ed19828d5eeb942faca sio:SIO_000628 miriam-gene:27286, lld:C0014544; a sio:SIO_001121 . } dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_provenance { dgn-np:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_assertion dcterms:description "[Previous studies have shown that uPAR(-/-) knock-out mice exhibited enhanced susceptibility to epileptic seizures and had brain cortical anomalies consistent with altered neuronal migration and maturation, all features that are reminiscent to the phenotypes caused by SRPX2 mutations.]. 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:18718938; 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:NP887766.RAETVS51bfcKN3JZJ6S2HGVPOneTzY0mNF_q9tkN0lVF0130_publicationInfo { this: dcterms:created "2015-08-25T14:46:41+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" . }