@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM> .
@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:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_head {
  this: np:hasAssertion dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_assertion;
    np:hasProvenance dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_provenance;
    np:hasPublicationInfo dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_assertion a np:Assertion .
  
  dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_provenance a np:Provenance .
  
  dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_assertion {
  miriam-gene:10395 a ncit:C16612 .
  
  lld:C0376358 a ncit:C7057 .
  
  dgn-gda:DGN2a21c83a432b51ba86bb680222b77e31 sio:SIO_000628 miriam-gene:10395, lld:C0376358;
    a sio:SIO_001121 .
}

dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_provenance {
  dgn-np:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_assertion dcterms:description
      "[These results show that the transcriptional silencing of DLC-1 by two epigenetic mechanisms is common and may be involved in the pathogenesis of prostate carcinomas and benign prostatic hyperplasias and could have potential clinical application in the early detection and gene therapy of prostate cancer.]. 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:16533763;
    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:NP460540.RApknuHFb2_tt5_96PyPu5NRrAYm-CIbW2HMH0CktTPiM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}