@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ> .
@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:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_head {
  this: np:hasAssertion dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion;
    np:hasProvenance dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_provenance;
    np:hasPublicationInfo dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion a np:Assertion .
  
  dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_provenance a np:Provenance .
  
  dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion {
  miriam-gene:4139 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN2867a183fcf4fa019c05f3b0c674468e sio:SIO_000628 miriam-gene:4139, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_provenance {
  dgn-np:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_assertion dcterms:description
      "[Recently, however, it has been proposed that differential epigenetic variability may mark genes that contribute to the risk of complex genetic diseases like cancer and that identification of risk and early detection markers may therefore benefit from statistics based on differential variability.]. 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:22492641;
    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:NP546359.RAulY1dtMn2XwXsYjgb2c-lkbpy4EYsNdT8z9Je9Px7bQ130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:03+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" .
}