@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo> .
@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:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_head {
  this: np:hasAssertion dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_assertion ;
    np:hasProvenance dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_provenance ;
    np:hasPublicationInfo dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_assertion a np:Assertion .
  dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_provenance a np:Provenance .
  dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_assertion {
  miriam-gene:4023 a ncit:C16612 .
  lld:C0011854 a ncit:C7057 .
  dgn-gda:DGNd8fa0eb41378c35be4c50a017d222765 sio:SIO_000628 miriam-gene:4023 , lld:C0011854 ;
    a sio:SIO_001121 .
}
dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_provenance {
  dgn-np:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_assertion dcterms:description "[Comparing individuals who were most susceptible to ON (those with an onset before 20 years duration of type 1 diabetes and before the development of other advanced complications) with the least susceptible (late or no occurrence of ON despite the development of other advanced complications) revealed otherwise undetected genetic associations [that is, apolipoprotein E (Apo E), angtiotensin-converting enzyme insertion/deletion (ACE I/D), and lipoprotein lipase (LPL) HindIII polymorphism) with odds ratios ranging from 2.9 to 7.1.]. 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:12164879 ;
    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:NP908252.RA497VUFhBrlhtUYwvARVLPxqsGEa4GVVqhcqkmxv5iuo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:17+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" .
}