@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798> .
@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:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_head {
  this: np:hasAssertion dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_assertion;
    np:hasProvenance dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_provenance;
    np:hasPublicationInfo dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_assertion a np:Assertion .
  
  dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_provenance a np:Provenance .
  
  dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_assertion {
  miriam-gene:6401 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGN79d242d2e20c6ee4ee2853e1e4e3aa7e sio:SIO_000628 miriam-gene:6401, lld:C0011849;
    a sio:SIO_001121 .
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dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_provenance {
  dgn-np:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_assertion dcterms:description
      "[We examined whether variation in the gene for E-selectin (SELE), a biomarker of endothelial dysfunction, was associated with levels of E-selectin or diabetes quantitative traits (including fasting levels of insulin and hemoglobin A(1c)) in 719 nondiabetic participants of the Nurses' Health Study or with risk of diabetes in 602 incident (over 10 years of follow-up) cases and 655 control women matched for age, race, and fasting status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP373082.RAzrjXOYfnYPBRDXwdgOFXATUdnTA4bfwa1ivV_Ef6798130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
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