@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4> .
@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:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_head {
  this: np:hasAssertion dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_assertion;
    np:hasProvenance dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_provenance;
    np:hasPublicationInfo dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_assertion a np:Assertion .
  
  dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_provenance a np:Provenance .
  
  dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_assertion {
  miriam-gene:2101 a ncit:C16612 .
  
  lld:C0018801 a ncit:C7057 .
  
  dgn-gda:DGNca2717138d9be7787c690e67c9fa3912 sio:SIO_000628 miriam-gene:2101, lld:C0018801;
    a sio:SIO_001121 .
}

dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_provenance {
  dgn-np:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_assertion dcterms:description
      "[Overall, our results implicate PGC-1alpha and ERRalpha in the pathophysiology of human heart failure, and define dynamic target gene sets sharing known interrelated regulatory mechanisms capable of contributing to the mitochondrial dysfunction characteristic of this disease process.]. 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:19061896;
    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:NP190840.RAXHjOwhsD1v8XT0RSS6N0fLaDi3UpEiTg7E_o2-3nur4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}