@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54> .
@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:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_head {
  this: np:hasAssertion dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_assertion;
    np:hasProvenance dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_provenance;
    np:hasPublicationInfo dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_assertion a np:Assertion .
  
  dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_provenance a np:Provenance .
  
  dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_assertion {
  miriam-gene:10062 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN17001770695c49359c215575430d05b9 sio:SIO_000628 miriam-gene:10062, lld:C0011860;
    a sio:SIO_001121 .
}

dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_provenance {
  dgn-np:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_assertion dcterms:description
      "[One thousand five hundred seventy-four subjects of European ancestry with elevated risk for type 2 diabetes were genotyped for the two NR1H2 single nucleotide polymorphisms (SNPs) rs2248949 and rs1405655 and for the four NR1H3 SNPs rs11039149, rs3758673, rs12221497 and rs2279238, and association studies with metabolic traits were performed.]. 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:21042792;
    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:NP546461.RAjnCaZKtkWrT8FiDoP8YhWODKwc-3b8k1UlWEfgRHA54130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:29+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" .
}