@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug> .
@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:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_head {
  this: np:hasAssertion dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_assertion;
    np:hasProvenance dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_provenance;
    np:hasPublicationInfo dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_assertion a np:Assertion .
  
  dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_provenance a np:Provenance .
  
  dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_assertion {
  miriam-gene:864 a ncit:C16612 .
  
  lld:C0014175 a ncit:C7057 .
  
  dgn-gda:DGN05670d771d71229c4eff499d1b3ad163 sio:SIO_000628 miriam-gene:864, lld:C0014175;
    a sio:SIO_001121 .
}

dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_provenance {
  dgn-np:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_assertion dcterms:description
      "[Negative protein expression and abnormal RUNX3 methylation in the eutopic endometrium could be used as diagnostic markers in patients with ovarian EM who may be at an increased risk of developing EAOC.]. 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:25333219;
    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:NP1231058.RA-rMXYPbQFS79yFiTUsjCIh8ooRX5xB1RfESD6m4U6Ug130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:04+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" .
}