@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4> .
@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:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_head {
  this: np:hasAssertion dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_assertion;
    np:hasProvenance dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_provenance;
    np:hasPublicationInfo dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_assertion a np:Assertion .
  
  dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_provenance a np:Provenance .
  
  dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0010481 a ncit:C7057 .
  
  dgn-gda:DGN454d63c5fbe7075f9d74ef0060af6742 sio:SIO_000628 miriam-gene:1029, lld:C0010481;
    a sio:SIO_001121 .
}

dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_provenance {
  dgn-np:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_assertion dcterms:description
      "[To our knowledge this is the first report that describes an intrinsic molecular change, namely methylation of the p16 gene CpG island, common to all three histological patterns associated with Cushing's disease.]. 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:15014032;
    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:NP257927.RAWAUCtcNe20RklvetC53_U9WekUS0D_BLuvfvDRrizl4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:24+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" .
}