@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY> .
@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:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_head {
  this: np:hasAssertion dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_assertion;
    np:hasProvenance dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_provenance;
    np:hasPublicationInfo dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_assertion a np:Assertion .
  
  dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_provenance a np:Provenance .
  
  dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGNa5f5cee808e3cadf8f431f7000a47b61 sio:SIO_000628 miriam-gene:7157, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_provenance {
  dgn-np:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_assertion dcterms:description
      "[The low frequencies of LOH and p53 alterations in sweat gland carcinomas contrasted with the multiple genetic defects normally observed in cutaneous squamous cell carcinomas, and may be partly explained by the relative protection of cutaneous appendages from ultraviolet light and other environmental mutagens.]. 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:10660129;
    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:NP154770.RAFEX8X_9A8Is-qIFZSbO7OuUEC_Sq8NdlzfFB-mCNiEY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}