@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw> .
@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:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_head {
  this: np:hasAssertion dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion;
    np:hasProvenance dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_provenance;
    np:hasPublicationInfo dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion a np:Assertion .
  
  dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_provenance a np:Provenance .
  
  dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion {
  miriam-gene:3320 a ncit:C16612 .
  
  lld:C0026769 a ncit:C7057 .
  
  dgn-gda:DGN2ca664afce42cb4c2eeba10671edec98 sio:SIO_000628 miriam-gene:3320, lld:C0026769;
    a sio:SIO_001121 .
}

dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_provenance {
  dgn-np:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_assertion dcterms:description
      "[Molecular mechanism of GS unresponsiveness in some patients with multiple sclerosis might be related to increased presence of hsp90 in the GR cytoplasmic complex, leading to the inhibition of GR translocation to nucleus and reduction in its transcription.]. 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:18573821;
    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:NP902650.RA2kHYVGuNuCuFpe_diUlo8unjM2-6bWw6fMBcGRjmKbw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:14+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" .
}