@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_head {
  this: np:hasAssertion dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_assertion;
    np:hasProvenance dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_provenance;
    np:hasPublicationInfo dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_assertion a np:Assertion .
  
  dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_provenance a np:Provenance .
  
  dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGN779d0276548f61b98a2c6682bed6d2a9 sio:SIO_000628 miriam-gene:7157, lld:C0596263;
    a sio:SIO_001122 .
}

dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_provenance {
  dgn-np:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_assertion dcterms:description
      "[Therefore, the creation of this mutator phenotype by missense-type p53 mutations implies that a more direct mechanism, apart from changes of cell cycle kinetics or cell death, may be responsible for the selection of certain p53 point mutations, which eventually result in the tumorigenesis of the cell.]. 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:8752146;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1355267.RAiqgf1dGm4w2Tq7gzCOFWpWg0Os_RqeJkZKxc-MV82fc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:52:00+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}