@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM> .
@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:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_head {
  this: np:hasAssertion dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_assertion;
    np:hasProvenance dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_provenance;
    np:hasPublicationInfo dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_assertion a np:Assertion .
  
  dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_provenance a np:Provenance .
  
  dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_assertion {
  miriam-gene:7299 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGNc7eb32fc6a40ea8f7f0f1ef794db0ff0 sio:SIO_000628 miriam-gene:7299, lld:C0376358;
    a sio:SIO_001122 .
}

dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_provenance {
  dgn-np:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_assertion dcterms:description
      "[Our data show for the first time, that allelism in genes linked with skin pigment synthesis is associated with prostate cancer risk possibly because it mediates the protective effects of UV. Importantly, susceptibility is associated with an interaction between host predisposition and exposure.]. 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:11720436;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP58893.RAEtujkxQkHJPEUgbQHMnPoOCWxnPjcT_WzY6nPlfOKHM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}