@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:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_head { this: np:hasAssertion dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_assertion; np:hasProvenance dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_provenance; np:hasPublicationInfo dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_publicationInfo; a np:Nanopublication . dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_assertion a np:Assertion . dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_provenance a np:Provenance . dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_publicationInfo a np:PublicationInfo . } dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_assertion { miriam-gene:6335 a ncit:C16612 . lld:C1720983 a ncit:C7057 . dgn-gda:DGN1d9d43977b422d42ba534605d7c4869e sio:SIO_000628 miriam-gene:6335, lld:C1720983; a sio:SIO_001121 . } dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_provenance { dgn-np:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_assertion dcterms:description "[This contributes to the clinical and neurophysiological characteristic of the sodium channel Nav1.7 channelopathy and expand our genetic knowledge which might provide more accurate and comprehensive clinical electrophysiological and genetic information.]. 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:24188911; 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:NP1124793.RAnaKSfO1ETGqjBmWPgh_ZkQ2Y9EeX6Ex5JpVQEhEkP5M130_publicationInfo { this: dcterms:created "2016-05-13T12:50:16+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" . }