@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs> .
@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:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_head {
  this: np:hasAssertion dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion;
    np:hasProvenance dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_provenance;
    np:hasPublicationInfo dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion a np:Assertion .
  
  dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_provenance a np:Provenance .
  
  dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion {
  miriam-gene:7422 a ncit:C16612 .
  
  lld:C0035320 a ncit:C7057 .
  
  dgn-gda:DGN375879e8f97753834259791e72fa7001 sio:SIO_000628 miriam-gene:7422, lld:C0035320;
    a sio:SIO_001123 .
}

dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_provenance {
  dgn-np:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_assertion dcterms:description
      "[Vector-based vascular endothelial growth factor 165 (VEGF) (165) targeted siRNA expression system (pSilencer (siVEGF)) was used to investigate the ability to inhibit VEGF (165) expression in vitro and suppresses retinal neovascularization.]. 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:18978955;
    prov:wasDerivedFrom dgn-void:lhgdn-20090331;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:lhgdn-20090331 pav:importedOn "2009-03-31"^^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:NP150248.RA18CMbcmI21wXrZpzFOi0LjKJEG7SR5ewsWOnh9a9ofs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:19+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" .
}