@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_head {
  this: np:hasAssertion dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_assertion;
    np:hasProvenance dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_provenance;
    np:hasPublicationInfo dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_assertion a np:Assertion .
  
  dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_provenance a np:Provenance .
  
  dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_assertion {
  miriam-gene:6328 a ncit:C16612 .
  
  lld:C0014544 a ncit:C7057 .
  
  dgn-gda:DGNa8be9b248c57125945eddd579e771df7 sio:SIO_000628 miriam-gene:6328, lld:C0014544;
    a sio:SIO_001121 .
}

dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_provenance {
  dgn-np:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_assertion dcterms:description
      "[Our data from the Hong Kong and Malaysia cohorts showed no significant allele, genotype and haplotype association of polymorphisms in the SCN1A, SCN2A, and SCN3A genes with drug responsiveness in 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:23859570;
    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:NP682767.RAXo94ZQMTlhdhAt0tl9uaZadw1HqUIgatQK2nQU9OYyg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:44:31+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetv3.0rdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}