@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw> .
@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:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_head {
  this: np:hasAssertion dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_assertion;
    np:hasProvenance dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_provenance;
    np:hasPublicationInfo dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_assertion a np:Assertion .
  
  dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_provenance a np:Provenance .
  
  dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_assertion {
  miriam-gene:2908 a ncit:C16612 .
  
  lld:C0010068 a ncit:C7057 .
  
  dgn-gda:DGN0136654868752b5b8b8703591f693bf2 sio:SIO_000628 miriam-gene:2908, lld:C0010068;
    a sio:SIO_001121 .
}

dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_provenance {
  dgn-np:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_assertion dcterms:description
      "[A single-nucleotide polymorphism (SNP) in the human glucocorticoid receptor (hGR) N363S (rs6195) has been the focus of several clinical studies, and some epidemiological data link this SNP to increased glucocorticoid sensitivity, coronary artery disease, and increased body mass index.]. 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:17535992;
    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:NP846972.RAyzRLE9DHhvWXyr50g_H7rpb4aAwiCqOLN2U9RX5DLtw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:38+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" .
}