@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM> .
@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:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_head {
  this: np:hasAssertion dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_assertion;
    np:hasProvenance dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_provenance;
    np:hasPublicationInfo dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_assertion a np:Assertion .
  
  dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_provenance a np:Provenance .
  
  dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_assertion {
  miriam-gene:7421 a ncit:C16612 .
  
  lld:C0030521 a ncit:C7057 .
  
  dgn-gda:DGN5aa35b0e9ba66fc9850f1e2ab177b5fa sio:SIO_000628 miriam-gene:7421, lld:C0030521;
    a sio:SIO_001121 .
}

dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_provenance {
  dgn-np:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_assertion dcterms:description
      "[In order to understand the role of aberrant DNA promoter methylation in the pathogenesis of parathyroid tumors, we have quantified the CpG island promoter methylation density of several candidate genes including APC (promoter 1A and 1B), β-catenin (CTNNB1), CASR, CDC73/HRPT2, MEN1, P16 (CDKN2A), PAX1, RASSF1A, SFRP1 and VDR in 72 parathyroid tumors and 3 normal parathyroid references using bisulfite pyrosequencing.]. 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:23764768;
    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:NP483395.RAv933DZ4pT0PQo3XXTnA8M5QuRYSlxUjNShRFmCmaCKM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:49+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" .
}