@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_head {
  this: np:hasAssertion dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_assertion;
    np:hasProvenance dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_provenance;
    np:hasPublicationInfo dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_assertion a np:Assertion .
  
  dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_provenance a np:Provenance .
  
  dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_assertion {
  miriam-gene:213 a ncit:C16612 .
  
  lld:C0011860 a ncit:C7057 .
  
  dgn-gda:DGN7ef3034ba899b2374e27487c1eed38e2 sio:SIO_000628 miriam-gene:213, lld:C0011860;
    a sio:SIO_001122 .
}

dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_provenance {
  dgn-np:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_assertion dcterms:description
      "[We investigated whether the coronary artery disease (CAD) locus on chromosome 9p21 (as represented by single nucleotide polymorphism rs2383206) is associated with low estimated glomerular filtration rate (eGFR) or increased urinary albumin excretion in patients with Type 2 diabetes mellitus (T2DM).]. 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:22622453;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP233398.RAGlS_YQNMYILKv_WlRTsqApAQPevJEqYY8DrELO8AqhA130_publicationInfo {
  this: dcterms:created "2015-08-25T14:39:52+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}