@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg> .
@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:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_head {
  this: np:hasAssertion dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion ;
    np:hasProvenance dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_provenance ;
    np:hasPublicationInfo dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion a np:Assertion .
  dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_provenance a np:Provenance .
  dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion {
  miriam-gene:6513 a ncit:C16612 .
  lld:C0020615 a ncit:C7057 .
  dgn-gda:DGN24697ef8c29fe29200fe2274bf979b2d sio:SIO_000628 miriam-gene:6513 , lld:C0020615 ;
    a sio:SIO_001121 .
}
dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_provenance {
  dgn-np:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_assertion dcterms:description "[Because glucose transport across these barriers is mediated exclusively by the sodium-independent glucose transporter GLUT1, changes in endothelial glucose transport and GLUT1 abundance in the barriers of the brain and retina may have profound consequences on glucose delivery to these tissues and major implications in the development of two major diabetic complications, namely insulin-induced hypoglycemia and diabetic retinopathy.]. 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:10495475 ;
    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:NP879487.RADJd1u6l55G-VZGWE07vvqgDwgV_rr5GeG-Rm8ZK8kmg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:57+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" .
}