@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk> .
@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:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_head {
  this: np:hasAssertion dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_assertion;
    np:hasProvenance dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_provenance;
    np:hasPublicationInfo dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_assertion a np:Assertion .
  
  dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_provenance a np:Provenance .
  
  dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_assertion {
  miriam-gene:3845 a ncit:C16612 .
  
  lld:C0345905 a ncit:C7057 .
  
  dgn-gda:DGN8ec8e944afb069150564e476b4a5f42b sio:SIO_000628 miriam-gene:3845, lld:C0345905;
    a sio:SIO_001121 .
}

dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_provenance {
  dgn-np:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_assertion dcterms:description
      "[Compared to ICC that was not associated with Thorotrast, the frequency of mutation of the KRAS gene was lower, while that of the TP53 gene was more than two times higher.]. 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:10564951;
    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:NP936016.RA8dvrrV70zn8P6aPwYRlUt3jbrrPeSFGVi44w36KGPIk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:33+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" .
}