@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw> .
@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:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_head {
  this: np:hasAssertion dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_assertion;
    np:hasProvenance dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_provenance;
    np:hasPublicationInfo dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_assertion a np:Assertion .
  
  dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_provenance a np:Provenance .
  
  dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_assertion {
  miriam-gene:56259 a ncit:C16612 .
  
  lld:C1168401 a ncit:C7057 .
  
  dgn-gda:DGN28011a4bccd20e5e513ebc6baaefeef4 sio:SIO_000628 miriam-gene:56259, lld:C1168401;
    a sio:SIO_001121 .
}

dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_provenance {
  dgn-np:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_assertion dcterms:description
      "[To understand the association of candidate tumour suppressor genes SH3GL2, p16(INK4a), p14(ARF), and p15(INK4b) in the pathogenesis of head and neck squamous cell carcinoma (HNSCC), we studied the deletion, mutation, and methylation of these genes in 61 dysplastic lesions and 94 HNSCC samples.]. 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:19023882;
    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:NP660951.RAS7t1azaD02n-vQgLivmxlu5Mpv16RuYjjaEj95WpmMw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:39+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" .
}