@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA> .
@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:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_head {
  this: np:hasAssertion dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_assertion;
    np:hasProvenance dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_provenance;
    np:hasPublicationInfo dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_assertion a np:Assertion .
  
  dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_provenance a np:Provenance .
  
  dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_assertion {
  miriam-gene:6667 a ncit:C16612 .
  
  lld:C0007134 a ncit:C7057 .
  
  dgn-gda:DGN28572fc73ef8d8b9a5c98b725413978d sio:SIO_000628 miriam-gene:6667, lld:C0007134;
    a sio:SIO_001121 .
}

dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_provenance {
  dgn-np:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_assertion dcterms:description
      "[DNase-I footprint and band-shift analysis demonstrated that Sp1 and HIF-1alpha proteins in nuclear extracts of RCC cells bind to the CAIX promoter and mutations in the most proximal Sp1 binding element or HIF binding element completely abolished CAIX promoter activity, indicating their critical importance for the activation of G250 expression in RCC.]. 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:15184875;
    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:NP693817.RAXq5CmNtQNtphsStO_He-0TudeUdlhYhAi6RF9LdVadA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:02+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" .
}