@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:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_head { this: np:hasAssertion dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_assertion; np:hasProvenance dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_provenance; np:hasPublicationInfo dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_publicationInfo; a np:Nanopublication . dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_assertion a np:Assertion . dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_provenance a np:Provenance . dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_publicationInfo a np:PublicationInfo . } dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_assertion { miriam-gene:9211 a ncit:C16612 . lld:C0009952 a ncit:C7057 . dgn-gda:DGNbb675b52c0740cf6c020582a00abf06d sio:SIO_000628 miriam-gene:9211, lld:C0009952; a sio:SIO_001121 . } dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_provenance { dgn-np:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_assertion dcterms:description "[Since 1995, positional cloning strategies in multigenerational families with autosomal dominant transmission have revealed 11 genes (KCNQ2, KCNQ3, CHRNA4, CHRNA2, CHRNB2, SCN1B, SCN1A, SCN2A, GABRG2, GABRA1, and LGI1) and numerous loci for febrile seizures and 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:20832659; 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:NP838474.RAjbFovHDtcoWpBlvM6hAcdTTW98GhkuXOU9krA3NGlWk130_publicationInfo { this: dcterms:created "2016-05-13T12:48:05+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" . }