@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:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_head { this: np:hasAssertion dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_assertion; np:hasProvenance dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_provenance; np:hasPublicationInfo dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_publicationInfo; a np:Nanopublication . dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_assertion a np:Assertion . dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_provenance a np:Provenance . dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_publicationInfo a np:PublicationInfo . } dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_assertion { miriam-gene:3342 a ncit:C16612 . lld:C0014544 a ncit:C7057 . dgn-gda:DGN495a13de17848fd2a7a4ca883326feb2 sio:SIO_000628 miriam-gene:3342, lld:C0014544; a sio:SIO_001121 . } dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_provenance { dgn-np:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_assertion dcterms:description "[We conclude that array CGH be considered an important investigation in adults with complicated epilepsy and, at least at present for selected patients, should join the diagnostic repertoire of clinical history and examination, neuroimaging, electroencephalography and other indicated investigations in generating a more complete formulation of an individual's epilepsy.]. 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:22342432; 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:NP961480.RAUgAtWKCNveU_RHMPoG0t5kDi3WmAGrQ-6mcOkEBd87g130_publicationInfo { this: dcterms:created "2016-05-13T12:49:00+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 "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }