@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do> .
@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:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_head {
  this: np:hasAssertion dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_assertion;
    np:hasProvenance dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_provenance;
    np:hasPublicationInfo dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_assertion a np:Assertion .
  
  dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_provenance a np:Provenance .
  
  dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_assertion {
  miriam-gene:2908 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN78badacda056f6595357fb65070827ea sio:SIO_000628 miriam-gene:2908, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_provenance {
  dgn-np:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_assertion dcterms:description
      "[Comparisons to natural glucocorticoid receptor mutants in the familial glucocorticoid resistance syndrome and steroid resistant leukemias suggest that amino acid substitutions at highly conserved residues may cause severe functional defects and serious illness, while changes at less conserved sites produce lesser alterations and milder disease.]. 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:10898924;
    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:NP693716.RAQ2Up2ue-hohRqRLG_apmvuuE_od1TxVg5SWC9SeZ5Do130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:01+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" .
}