@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA> .
@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:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_head {
  this: np:hasAssertion dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_assertion;
    np:hasProvenance dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_provenance;
    np:hasPublicationInfo dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_assertion a np:Assertion .
  
  dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_provenance a np:Provenance .
  
  dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_assertion {
  miriam-gene:5989 a ncit:C16612 .
  
  lld:C0017638 a ncit:C7057 .
  
  dgn-gda:DGNfe9f9e5a192fd1c9bb0155d8c779b93a sio:SIO_000628 miriam-gene:5989, lld:C0017638;
    a sio:SIO_001121 .
}

dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_provenance {
  dgn-np:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_assertion dcterms:description
      "[We also demonstrated that the isolated CpG island located in the seventh intron of the RFX1 gene had enhancer activity and was hypermethylated in all of the glioma tissues and cell lines analysed, but not in normal brains or lymphocytes.]. 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:15334059;
    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:NP316245.RAmA4_nWQIGRM_8Oxf1Ro5vb2GeuYQMOUITr4dS9O2QXA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:01+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" .
}