@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0> .
@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:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_head {
  this: np:hasAssertion dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_assertion;
    np:hasProvenance dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_provenance;
    np:hasPublicationInfo dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_assertion a np:Assertion .
  
  dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_provenance a np:Provenance .
  
  dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0699893 a ncit:C7057 .
  
  dgn-gda:DGN71f2fec7cb91ba6d1e1514e049f44f4d sio:SIO_000628 miriam-gene:7157, lld:C0699893;
    a sio:SIO_001121 .
}

dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_provenance {
  dgn-np:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_assertion dcterms:description
      "[Multiple and distinct p53 mutations were detected by DNA sequence analysis in tumor and adjacent nonmalignant skin samples from eight patients with nonmelanoma skin cancer of the head and neck, providing unambiguous evidence for field cancerization.]. 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:7627969;
    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:NP207282.RAQHfEF5Y6MsvV9ftK-UhVlCXnjgN3VvdpVJ2oK-GTb_0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:54+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" .
}