@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4> .
@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:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_head {
  this: np:hasAssertion dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_assertion;
    np:hasProvenance dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_provenance;
    np:hasPublicationInfo dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_assertion a np:Assertion .
  
  dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_provenance a np:Provenance .
  
  dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_assertion {
  miriam-gene:5972 a ncit:C16612 .
  
  lld:C0232197 a ncit:C7057 .
  
  dgn-gda:DGN7540095e94eb1c1ab6d8298c97d05f60 sio:SIO_000628 miriam-gene:5972, lld:C0232197;
    a sio:SIO_001121 .
}

dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_provenance {
  dgn-np:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_assertion dcterms:description
      "[By genetic association study, some genetic variants or polymorphisms related to the mechanism of AF have been found to be associated with common AF, including genes encoding for subunits of potassium or sodium channels, sarcolipin gene, renin-angiotensin system gene, connexin-40 gene, endothelial nitric oxide synthase gene, and interleukin-10 gene.]. 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:18634977;
    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:NP709848.RAbuFot-IX2fKqCQ81-qtdfPwTA6WeTU59U-W47Uz0Qf4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}