@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg> .
@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:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_head {
  this: np:hasAssertion dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_assertion;
    np:hasProvenance dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_provenance;
    np:hasPublicationInfo dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_assertion a np:Assertion .
  
  dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_provenance a np:Provenance .
  
  dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_assertion {
  miriam-gene:3290 a ncit:C16612 .
  
  lld:C0010481 a ncit:C7057 .
  
  dgn-gda:DGNd26b5691183d2890df30212ee2e53518 sio:SIO_000628 miriam-gene:3290, lld:C0010481;
    a sio:SIO_001121 .
}

dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_provenance {
  dgn-np:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_assertion dcterms:description
      "[The aim of the present study was to explore presumed associations between the 83,557insA variant of the HSD11B1 gene and circulating hormone concentrations, bone turnover and bone mineral density (BMD) in patients with endogenous Cushing's syndrome (CS).]. 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:21111044;
    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:NP540843.RA2nh22dQual7wzifbc9LYrCxE6m6OBOHkV9NOfWhAHFg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:26+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" .
}