@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:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_head { this: np:hasAssertion dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_assertion; np:hasProvenance dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_provenance; np:hasPublicationInfo dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_publicationInfo; a np:Nanopublication . dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_assertion a np:Assertion . dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_provenance a np:Provenance . dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_publicationInfo a np:PublicationInfo . } dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_assertion { miriam-gene:9681 a ncit:C16612 . lld:C0014547 a ncit:C7057 . dgn-gda:DGN9c17ef7e88ee6f9c4f25fa366ccd674e sio:SIO_000628 miriam-gene:9681, lld:C0014547; a sio:SIO_001121 . } dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_provenance { dgn-np:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_assertion dcterms:description "[A particular focus is DEPDC5, the first gene for nonlesional focal epilepsy likely to be relevant to sporadic patients with focal epilepsies and those from small families, in contrast to rare large families with autosomal dominant focal epilepsies.]. 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:24615646; 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:NP828734.RAWlh-WyumM9LgIFKYtMdWWP0RRirEXdotP9C9MS8yBjA130_publicationInfo { this: dcterms:created "2015-08-25T14:46:02+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" . }