@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo> .
@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:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_head {
  this: np:hasAssertion dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion;
    np:hasProvenance dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_provenance;
    np:hasPublicationInfo dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion a np:Assertion .
  
  dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_provenance a np:Provenance .
  
  dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion {
  miriam-gene:6331 a ncit:C16612 .
  
  lld:C0037052 a ncit:C7057 .
  
  dgn-gda:DGN0aee6f5d8df6e0ec5e094456e74f71ed sio:SIO_000628 miriam-gene:6331, lld:C0037052;
    a sio:SIO_001121 .
}

dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_provenance {
  dgn-np:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_assertion dcterms:description
      "[Mutations in SCN5A, the gene encoding Na(v)1.5, have been linked to many cardiac phenotypes, including the congenital and acquired long QT syndrome, Brugada syndrome, conduction slowing, sick sinus 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:19744495;
    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:NP622352.RAF5XxD_OwMjR2UoOWnDM9tvh7WYHsHipCEIk6iz3aKSo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:16+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" .
}