@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI> .
@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:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_head {
  this: np:hasAssertion dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_assertion;
    np:hasProvenance dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_provenance;
    np:hasPublicationInfo dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_assertion a np:Assertion .
  
  dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_provenance a np:Provenance .
  
  dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGN749b719168e6d2a4699be8c5aa30d0f3 sio:SIO_000628 miriam-gene:6331, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_provenance {
  dgn-np:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_assertion dcterms:description
      "[Since the identification of the first SCN5A mutation associated with long QT syndrome in 1995, several mutations in this gene for the alpha subunit of the cardiac sodium channel have been identified in a heterogeneous subset of cardiac rhythm syndromes, including Brugada syndrome, progressive cardiac conduction defect, sick sinus node syndrome, atrial fibrillation and dilated cardiomyopathy.]. 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:19377496;
    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:NP219094.RAzKGAxe0BEzwVyaBtnSNXuhtdRHljoxLZ3okXmI_XHaI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:01+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" .
}