@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E> .
@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:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_head {
  this: np:hasAssertion dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_assertion;
    np:hasProvenance dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_provenance;
    np:hasPublicationInfo dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_assertion a np:Assertion .
  
  dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_provenance a np:Provenance .
  
  dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_assertion {
  miriam-gene:5308 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN75c44e37ebfa49a06e9ca4b92c45c3e1 sio:SIO_000628 miriam-gene:5308, lld:C0038454;
    a sio:SIO_001122 .
}

dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_provenance {
  dgn-np:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_assertion dcterms:description
      "[We discovered that variants previously shown to associate with atrial fibrillation (AF), rs2200733 and rs10033464, significantly associated with IS, with the strongest risk for CES. The association with noncardiogenic stroke is intriguing and suggests that atrial fibrillation may be underdiagnosed in patients presenting with stroke. This discovery may have implications for workup and treatment of IS.]. 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:18991354;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP94605.RASe0JC_RROZVyN5mK_qXcummdzVmMDEd36IDy3TKk-_E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:47+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" .
}