@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk> .
@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:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_head {
  this: np:hasAssertion dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_assertion;
    np:hasProvenance dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_provenance;
    np:hasPublicationInfo dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_assertion a np:Assertion .
  
  dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_provenance a np:Provenance .
  
  dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_assertion {
  miriam-gene:5727 a ncit:C16612 .
  
  lld:C0699893 a ncit:C7057 .
  
  dgn-gda:DGN75d2d1aec0a08b5ebd81dd6e148f276b sio:SIO_000628 miriam-gene:5727, lld:C0699893;
    a sio:SIO_001122 .
}

dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_provenance {
  dgn-np:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_assertion dcterms:description
      "[ Our results indicate an association between the eumelanin-to-phaeomelanin shift and a shift from the Pro/Pro genotype to Leu-containing genotypes. Failure to lose Pro during the shift to phaeomelanin may be associated with an increased population risk for BCC and increased individual risk for multiple BCC. During development of a tumour, the effect of Pro may be magnified by loss of the Leu allele.]. 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:15888139;
    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:NP52585.RA7TBxJ2wNc0orH5MuWb97N5CfPdw_UEPfVkvxZqY6fmk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}