@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE> .
@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:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_head {
  this: np:hasAssertion dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion;
    np:hasProvenance dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_provenance;
    np:hasPublicationInfo dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion a np:Assertion .
  
  dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_provenance a np:Provenance .
  
  dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion {
  miriam-gene:1284 a ncit:C16612 .
  
  lld:C3272363 a ncit:C7057 .
  
  dgn-gda:DGN7a96d1777913734adfdda72c483639d4 sio:SIO_000628 miriam-gene:1284, lld:C3272363;
    a sio:SIO_001121 .
}

dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_provenance {
  dgn-np:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_assertion dcterms:description
      "[We investigated whether variants within a larger set of oxidative phosphorylation (OXPHOS) genes encoded by both autosomal and mitochondrial DNA were associated with risk of IS and, based on our results, extended our investigation to intracerebral hemorrhage (ICH).]. 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:23362085;
    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:NP524594.RAdKOAc2uiR7FyJgJVFM6_Q9eZUeo21ZfML-nuBn2LlWE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:14+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" .
}