@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8> .
@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:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_head {
  this: np:hasAssertion dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_assertion;
    np:hasProvenance dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_provenance;
    np:hasPublicationInfo dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_assertion a np:Assertion .
  
  dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_provenance a np:Provenance .
  
  dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGN608c58bc2d5ff742d2df4ca5bf2c3e6c sio:SIO_000628 miriam-gene:7248, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_provenance {
  dgn-np:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_assertion dcterms:description
      "[The frequent changes occurring in the p53 pathway in HNSCC imply that molecular genetic and immunocytochemical analysis of this critical tumour suppressor network may be of diagnostic and prognostic utility in the clinical management of HNSCC.]. 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:12618194;
    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:NP385671.RAZeaMEa5R20ABcgTG1xrVwXyPHV5ZGXGbN-a2fRLOer8130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:40+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" .
}