@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g> .
@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:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_head {
  this: np:hasAssertion dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion;
    np:hasProvenance dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_provenance;
    np:hasPublicationInfo dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion a np:Assertion .
  
  dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_provenance a np:Provenance .
  
  dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion {
  miriam-gene:11197 a ncit:C16612 .
  
  lld:C0025218 a ncit:C7057 .
  
  dgn-gda:DGN0bae914cc27efc6d63af5ece37249a6c sio:SIO_000628 miriam-gene:11197, lld:C0025218;
    a sio:SIO_001121 .
}

dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_provenance {
  dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion dcterms:description
      "[Collectively, WIF-1 downregulation, which may occur in epidermal keratinocytes and in dermal fibroblasts, is involved in melasma development because of the stimulation of melanogenesis and melanosome transfer through upregulation of the canonical and the noncanonical Wnt signaling pathway.]. 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:22951732;
    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:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}