@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4> .
@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:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_head {
  this: np:hasAssertion dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_assertion;
    np:hasProvenance dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_provenance;
    np:hasPublicationInfo dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_assertion a np:Assertion .
  
  dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_provenance a np:Provenance .
  
  dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0278996 a ncit:C7057 .
  
  dgn-gda:DGN7c64c2720213c074b09f44241cb10765 sio:SIO_000628 miriam-gene:1029, lld:C0278996;
    a sio:SIO_001121 .
}

dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_provenance {
  dgn-np:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_assertion dcterms:description
      "[In order to investigate p16 alterations in head and neck cancer (HNC) we analyzed 70 primary tumors of the larynx, pharynx and oral cavity including their corresponding normal mucosa for mutation inactivation by direct sequencing exon 2.]. 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:10373639;
    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:NP190922.RAPfDy2lknzqBXMvpPDnJpxBfA7IoQPSeLbxcazqDw6r4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}