@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw> .
@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:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_head {
  this: np:hasAssertion dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion;
    np:hasProvenance dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_provenance;
    np:hasPublicationInfo dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion a np:Assertion .
  
  dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_provenance a np:Provenance .
  
  dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion {
  miriam-gene:5925 a ncit:C16612 .
  
  lld:C0001418 a ncit:C7057 .
  
  dgn-gda:DGNfdb1bb51cc28c9f1a2ee793589c9c447 sio:SIO_000628 miriam-gene:5925, lld:C0001418;
    a sio:SIO_001121 .
}

dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_provenance {
  dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion dcterms:description
      "[We found that half (7 of 14) of lung adenocarcinomas with high telomerase activity showed neither TP53 nor RB1 deletion, while all squamous cell carcinomas and SCLCs with high telomerase activity showed loss of heterozygosity of at least one, if not both, of these suppressor oncogenes, indicating that these genetic aberrations are not required in activation of telomerase in a unique subset of adenocarcinoma.]. 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:17487398;
    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:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:46+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" .
}