@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE> .
@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:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_head {
  this: np:hasAssertion dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_assertion;
    np:hasProvenance dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_provenance;
    np:hasPublicationInfo dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_assertion a np:Assertion .
  
  dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_provenance a np:Provenance .
  
  dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_assertion {
  miriam-gene:6517 a ncit:C16612 .
  
  lld:C0020459 a ncit:C7057 .
  
  dgn-gda:DGNc3946d3f0054b4071c1efae5182b2534 sio:SIO_000628 miriam-gene:6517, lld:C0020459;
    a sio:SIO_001121 .
}

dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_provenance {
  dgn-np:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_assertion dcterms:description
      "[Here we show in a model of chronic hyperinsulinemia that adipocytes develop selective insulin resistance in which translocation of the GLUT4 glucose transporter to the cell surface is blunted yet nuclear exclusion of the FoxO1 transcription factor is preserved, rendering uncoupled insulin-controlled carbohydrate and lipid metabolisms.]. 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:21646544;
    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:NP640003.RAAz6IJyQ88LNFqCB8aecSVMVK3QmmEWnFNrXTqVzqGzE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:26+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" .
}