@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_head {
  this: np:hasAssertion dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_assertion;
    np:hasProvenance dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_provenance;
    np:hasPublicationInfo dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_assertion a np:Assertion .
  
  dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_provenance a np:Provenance .
  
  dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_assertion {
  miriam-gene:5468 a ncit:C16612 .
  
  lld:C0023787 a ncit:C7057 .
  
  dgn-gda:DGN6c700a166805a1a25489a773e51c592d sio:SIO_000628 miriam-gene:5468, lld:C0023787;
    a sio:SIO_001121 .
}

dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_provenance {
  dgn-np:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_assertion dcterms:description
      "[To provide a broader context for how these mutations act to generate the clinical features of partial lipodystrophy we will review the basic biology of PPARγ and also survey the set PPARγ genetic variants that do not cause lipodystrophy, but are nonetheless associated with clinically related syndromes, specifically type 2 diabetes.]. 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:25460295;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1243599.RAd2ujb1S8Q1Hn7I-jndkGsD7N6RERq5JX-tG2qZ5a0oo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:09+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}