@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg> .
@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:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_head {
  this: np:hasAssertion dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion;
    np:hasProvenance dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_provenance;
    np:hasPublicationInfo dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion a np:Assertion .
  
  dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_provenance a np:Provenance .
  
  dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion {
  miriam-gene:1786 a ncit:C16612 .
  
  lld:C0525045 a ncit:C7057 .
  
  dgn-gda:DGN110ace59a51df12e3167c1a06243d387 sio:SIO_000628 miriam-gene:1786, lld:C0525045;
    a sio:SIO_001121 .
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dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_provenance {
  dgn-np:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_assertion dcterms:description
      "[Thus, our data suggest that the altered expression of DNMTs is state dependent and that the aberrant epigenetic gene regulations caused by the altered expression of DNMT1 and DNMT3B may be associated with the pathophysiology of mood disorders.]. 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:21592522;
    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:NP677978.RAeFjhIfC6U8jUcrFo40yU9XtWRiRA1ru6IM-LpIBaoYg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:49+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}