@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0> .
@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:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_head {
  this: np:hasAssertion dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion;
    np:hasProvenance dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_provenance;
    np:hasPublicationInfo dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion a np:Assertion .
  
  dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_provenance a np:Provenance .
  
  dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion {
  miriam-gene:1594 a ncit:C16612 .
  
  lld:C0011884 a ncit:C7057 .
  
  dgn-gda:DGN6b882356557c515aaf31591b646890b8 sio:SIO_000628 miriam-gene:1594, lld:C0011884;
    a sio:SIO_001121 .
}

dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_provenance {
  dgn-np:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_assertion dcterms:description
      "[After correcting for duration of disease, only the VDR gene BsmI genotypes showed significant association with cumulative prevalence of diabetic retinopathy, while no investigated genetic polymorphysms could reliably predict diabetic nephropathy.]. 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:20120526;
    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:NP437527.RAdvof2EZIuTgpFJo6BYaRYN8NHXYNrT0CWoQjGUUofd0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:19+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}