@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c> .
@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/v4.0.0/void/> .

dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_head {
  this: np:hasAssertion dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion;
    np:hasProvenance dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_provenance;
    np:hasPublicationInfo dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion a np:Assertion .
  
  dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_provenance a np:Provenance .
  
  dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion {
  miriam-gene:7020 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNb06e016b82970083ae2d687b95638b70 sio:SIO_000628 miriam-gene:7020, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_provenance {
  dgn-np:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_assertion dcterms:description
      "[We have identified aberrant CpG DNA methylation as an epigenetic mark associated with TFAP2A silencing in human melanoma that could have significant implications for the therapy of human melanoma using epigenetic modifying drugs.]. 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:25625848;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1258852.RA15pMNzkvQD1QaFaoU7_opMp3vHaJkIMxsNV_ItAGF4c130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:17+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}