@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_head {
  this: np:hasAssertion dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_assertion;
    np:hasProvenance dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_provenance;
    np:hasPublicationInfo dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_assertion a np:Assertion .
  
  dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_provenance a np:Provenance .
  
  dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_assertion {
  miriam-gene:5130 a ncit:C16612 .
  
  lld:C1306459 a ncit:C7057 .
  
  dgn-gda:DGN245e0f663063abb75152017b0fd62f85 sio:SIO_000628 miriam-gene:5130, lld:C1306459;
    a sio:SIO_001121 .
}

dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_provenance {
  dgn-np:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_assertion dcterms:description
      "[Our results corroborate that widespread DNA hypomethylation appears to be the driver in the derepression of CTA expression in cancer and furthermore, demonstrate that these hypomethylated domains are associated with the nuclear lamina-associated domains (LADS).]. 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:23522060;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP612736.RAoz0RRLlxaNNNTunq06NPFN79ptdj89Ub3RiHzRdQ1fA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:46+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}