@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8> .
@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:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_head {
  this: np:hasAssertion dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion;
    np:hasProvenance dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_provenance;
    np:hasPublicationInfo dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion a np:Assertion .
  
  dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_provenance a np:Provenance .
  
  dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion {
  miriam-gene:1540 a ncit:C16612 .
  
  lld:C1457883 a ncit:C7057 .
  
  dgn-gda:DGN0f89ae666b6ed72b5c743da02b4ab25e sio:SIO_000628 miriam-gene:1540, lld:C1457883;
    a sio:SIO_001121 .
}

dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_provenance {
  dgn-np:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_assertion dcterms:description
      "[In contrast with previous studies showing the development of benign tumors by mutations in the CYLD gene, here we provide evidence that the occurrence of mutations in the CYLD gene in tumorigenic epidermal cells (carrying previous mutations) increases the aggressiveness of carcinomas, mainly through enhancement of the expression of angiogenic factors, having therefore a key role in epidermal cancer malignancy.]. 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:20838385;
    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:NP277570.RAOn_M5SbqIQEmEvHUtYb045LYlljphaK8broW40Drhk8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:36+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" .
}