@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs> .
@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:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_head {
  this: np:hasAssertion dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion;
    np:hasProvenance dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_provenance;
    np:hasPublicationInfo dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion a np:Assertion .
  
  dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_provenance a np:Provenance .
  
  dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0027651 a ncit:C7057 .
  
  dgn-gda:DGNcdf3e5ede1e25a64a2e73c7c084b398c sio:SIO_000628 miriam-gene:7157, lld:C0027651;
    a sio:SIO_001122 .
}

dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_provenance {
  dgn-np:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_assertion dcterms:description
      "[We summarize here current knowledge on the respective roles of p53 mutagenesis and biological selection of mutations with specific functional characteristic in shaping the patterns and phenotypes of mutations observed in human cancers.]. 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:17401424;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP111390.RAGDHCDJlKfiDE0lD0kC0h0i7d3S2o7yfguvQC5b-H5cs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:57+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" .
}