@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I> .
@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:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_head {
  this: np:hasAssertion dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_assertion;
    np:hasProvenance dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_provenance;
    np:hasPublicationInfo dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_assertion a np:Assertion .
  
  dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_provenance a np:Provenance .
  
  dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNd9d7b3464444217c119317ce41830e86 sio:SIO_000628 miriam-gene:1029, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_provenance {
  dgn-np:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_assertion dcterms:description
      "[The lack of CDKN2A promoter mutations and the absence of transcriptional silencing in the germ line of this cohort of families suggest that mutations in the promoter and 5' UTR play a very limited role in melanoma predisposition.]. 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:11477665;
    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:NP325486.RA8sP5JVLQ0NKk8ybvfWkR8aOgdjDFsOGGzjtOouYi25I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:13+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" .
}