@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA> .
@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:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_head {
  this: np:hasAssertion dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_assertion;
    np:hasProvenance dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_provenance;
    np:hasPublicationInfo dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_assertion a np:Assertion .
  
  dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_provenance a np:Provenance .
  
  dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_assertion {
  miriam-gene:5445 a ncit:C16612 .
  
  lld:C0022658 a ncit:C7057 .
  
  dgn-gda:DGN08c59930d4ae9bc9c32b6098c77ed9f2 sio:SIO_000628 miriam-gene:5445, lld:C0022658;
    a sio:SIO_001122 .
}

dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_provenance {
  dgn-np:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_assertion dcterms:description
      "[The paraoxonase2 gene polymorphisms were significantly associated with diabetic nephropathy independent of traditional risk factors in Type II diabetic patients. The susceptibility to diabetic nephropathy was intensified by the degree of obesity. Pathophysiological pathways should be investigated and could be involved in insulin resistance or lipids metabolism or both.]. 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:11206400;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP52901.RA4EOQxjWgYwxUxQhBDtc61dVvKpjvOrBFyZqn_3pAuqA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:24+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" .
}