@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8> .
@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:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_head {
  this: np:hasAssertion dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion;
    np:hasProvenance dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_provenance;
    np:hasPublicationInfo dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion a np:Assertion .
  
  dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_provenance a np:Provenance .
  
  dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion {
  miriam-gene:6696 a ncit:C16612 .
  
  lld:C0017636 a ncit:C7057 .
  
  dgn-gda:DGN99187c7b9aa6dad5132293ea07b31d24 sio:SIO_000628 miriam-gene:6696, lld:C0017636;
    a sio:SIO_001121 .
}

dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_provenance {
  dgn-np:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_assertion dcterms:description
      "[Among a panel of known hypoxia-inducible genes, OPN and CA9 emerge as most consistently induced by in vitro hypoxia in human GBM cell lines and most specifically expressed in patient GBM tumor tissue, rendering these two genes attractive targets for hypoxia-directed treatment approaches.]. 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:17524506;
    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:NP849840.RAD_s9nw855Ug6XwHTIGarHwaLukpZj40Kw1a6nF5RYM8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:39+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" .
}