@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE> .
@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:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_head {
  this: np:hasAssertion dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_assertion ;
    np:hasProvenance dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_provenance ;
    np:hasPublicationInfo dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_assertion a np:Assertion .
  dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_provenance a np:Provenance .
  dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_assertion {
  miriam-gene:4846 a ncit:C16612 .
  lld:C1621958 a ncit:C7057 .
  dgn-gda:DGN8ac1ddf89a1a55de5afeb0fbd07dbb4d sio:SIO_000628 miriam-gene:4846 , lld:C1621958 ;
    a sio:SIO_001121 .
}
dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_provenance {
  dgn-np:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_assertion dcterms:description "[In either uninfected GBM cells or neural progenitor cells, thought to be the GBM precursor cells, HCMV infection or US28 overexpression was sufficient to promote secretion of biologically active VEGF and to activate multiple cellular kinases that promote glioma growth and invasion, including phosphorylated STAT3 (p-STAT3) and endothelial nitric oxide synthase (e-NOS).]. 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:21900396 ;
    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:NP832318.RARYIBDaxBBzTcxDrDCEbRkJQ1xFugDX4ok64QfIwSHsE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:29+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" .
}