@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI> .
@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:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_head {
  this: np:hasAssertion dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_assertion;
    np:hasProvenance dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_provenance;
    np:hasPublicationInfo dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_assertion a np:Assertion .
  
  dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_provenance a np:Provenance .
  
  dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_assertion {
  miriam-gene:1958 a ncit:C16612 .
  
  lld:C0029408 a ncit:C7057 .
  
  dgn-gda:DGN0868ad22e77d590230bb1a307bef6a27 sio:SIO_000628 miriam-gene:1958, lld:C0029408;
    a sio:SIO_001121 .
}

dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_provenance {
  dgn-np:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_assertion dcterms:description
      "[After regulatory network construction and regulatory impact factor analysis, we found that EGR1, NFE2L1, and NFYA were crucial TFs in the regulatory network of RA and NFYA, CBFB, CREB1, YY1 and PATZ1 were crucial TFs in the regulatory network of OA.]. 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:23296645;
    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:NP188127.RAQL8bfXljZQCFZ1HbD9NrRRAFd0unvLD-SOc7mW1iEVI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}