@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM> .
@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:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_head {
  this: np:hasAssertion dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion;
    np:hasProvenance dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_provenance;
    np:hasPublicationInfo dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion a np:Assertion .
  
  dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_provenance a np:Provenance .
  
  dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion {
  miriam-gene:5467 a ncit:C16612 .
  
  lld:C0242339 a ncit:C7057 .
  
  dgn-gda:DGN6a74d24ff73654497d5efa7d86434744 sio:SIO_000628 miriam-gene:5467, lld:C0242339;
    a sio:SIO_001121 .
}

dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_provenance {
  dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion dcterms:description
      "[Previous studies have identified a single-nucleotide polymorphism in the gene encoding peroxisome proliferator-activated receptor-delta (PPARD), rs2016520, that is associated with changes in metabolic disease in some but not all studies, which suggests that PPARD agonists may have therapeutic benefits for the treatment of metabolic disorders, including dyslipidemia, type 2 diabetes, and obesity.]. 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:20200337;
    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:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:59+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" .
}