@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA> .
@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:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_head {
  this: np:hasAssertion dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_assertion;
    np:hasProvenance dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_provenance;
    np:hasPublicationInfo dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_assertion a np:Assertion .
  
  dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_provenance a np:Provenance .
  
  dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_assertion {
  miriam-gene:4000 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN0123bd0aecc1bd8f9a68fa1b30785119 sio:SIO_000628 miriam-gene:4000, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_provenance {
  dgn-np:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_assertion dcterms:description
      "[Several exciting recent discoveries also point to a genome-scale disruption of the epigenome that involves large blocks of DNA hypomethylation, mutations of epigenetic modifier genes and alterations of heterochromatin in cancer (including large organized chromatin lysine modifications (LOCKs) and lamin-associated domains (LADs)), all of which increase epigenetic and gene expression plasticity.]. 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:23760024;
    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:NP865785.RA1Ncy4eohCk8rTIzU9FmUH5bdxegv3tZrrisQdJHdvSA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:49+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" .
}