@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU> .
@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:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_head {
  this: np:hasAssertion dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion;
    np:hasProvenance dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_provenance;
    np:hasPublicationInfo dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion a np:Assertion .
  
  dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_provenance a np:Provenance .
  
  dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion {
  miriam-gene:4089 a ncit:C16612 .
  
  lld:C0178874 a ncit:C7057 .
  
  dgn-gda:DGN71117e01fe250951e8040290d55bb422 sio:SIO_000628 miriam-gene:4089, lld:C0178874;
    a sio:SIO_001121 .
}

dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_provenance {
  dgn-np:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_assertion dcterms:description
      "[K-ras mutations frequently occur early, whereas changes in the expression and genetic integrity of the p16 gene appear in intermediate lesions, and the inactivation of the p53, DPC4 genes and activation of telomerase occur late in the neoplastic progression.]. 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:11490843;
    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:NP166897.RAYHimkPZcQ7aQAp3o0xkLDRD_6NdpJYQSHHfYRMlIXmU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:30+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" .
}