@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs> .
@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:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_head {
  this: np:hasAssertion dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_assertion ;
    np:hasProvenance dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_provenance ;
    np:hasPublicationInfo dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_assertion a np:Assertion .
  dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_provenance a np:Provenance .
  dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_assertion {
  miriam-gene:6513 a ncit:C16612 .
  lld:C0019562 a ncit:C7057 .
  dgn-gda:DGNe97cea12a369c7f6405c8fe71a4769eb sio:SIO_000628 miriam-gene:6513 , lld:C0019562 ;
    a sio:SIO_001121 .
}
dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_provenance {
  dgn-np:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_assertion dcterms:description "[Our data indicate that the Arg200Trp substitution impairs the interaction of VHL with HIF1alpha, reducing the rate of degradation of HIF1alpha and resulting in increased expression of downstream target genes including EPO (encoding erythropoietin), SLC2A1 (also known as GLUT1, encoding solute carrier family 2 (facilitated glucose transporter), member 1), TF (encoding transferrin), TFRC (encoding transferrin receptor (p90, CD71)) and VEGF (encoding vascular endothelial growth factor).]. 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:12415268 ;
    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:NP466627.RAliJC6hRb7-hgH3sC5hc6rIj3-IG4XjVkeIep4g62kCs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:40+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> ;
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    pav:version "v2.1.0.0" .
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}