@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4> .
@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:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_head {
  this: np:hasAssertion dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_assertion;
    np:hasProvenance dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_provenance;
    np:hasPublicationInfo dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_assertion a np:Assertion .
  
  dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_provenance a np:Provenance .
  
  dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_assertion {
  miriam-gene:5891 a ncit:C16612 .
  
  lld:C0011884 a ncit:C7057 .
  
  dgn-gda:DGN26d329c40584eb1942d609be6b23f309 sio:SIO_000628 miriam-gene:5891, lld:C0011884;
    a sio:SIO_001122 .
}

dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_provenance {
  dgn-np:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_assertion dcterms:description
      "[We previously reported the association of the Z-2 allele of the promoter dinucleotide repeat in the Aldose reductase (ALR2) gene, the (CCTTT) allele in the promoter of inductible nitric oxide synthase (iNOS) gene, and the (GT) promoter polymorphism in the tumor necrosis factor  (TNFB) gene with an increased risk for diabetic retinopathy (DR), and the Gly82Ser polymorphism in the receptor for advanced glycation end products (RAGE) gene and the (GT) allele of the TNFB gene with low-risk for DR in a hospital-based self-reported type 2 diabetes mellitus (T2DM) patients.]. 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:21067489;
    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:NP52386.RAle6opyiaDHcePNAQkATUI1egTuRTc_SaIAvSk1ve4t4130_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" .
}