@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_head {
  this: np:hasAssertion dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_assertion;
    np:hasProvenance dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_provenance;
    np:hasPublicationInfo dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_assertion a np:Assertion .
  
  dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_provenance a np:Provenance .
  
  dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_assertion {
  miriam-gene:6327 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGNb99165d2ab4a6f65821a094fdd5ee796 sio:SIO_000628 miriam-gene:6327, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_provenance {
  dgn-np:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_assertion dcterms:description
      "[Mutations in the cardiac sodium channel α, β1, β2 and β3 subunit genes (SCN5A, SCN1B, SCN2B and SCN3B) have been associated with AF, which suggests that mutations in the sodium channel β4 subunit gene, SCN4B, are also involved in the pathogenesis of AF.]. 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:23604097;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP295920.RAD0wnUSGjBI6zcUWcTYhIdYsD466Cs2tK-9WP50xIvPM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}