@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs> .
@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:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_head {
  this: np:hasAssertion dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_assertion;
    np:hasProvenance dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_provenance;
    np:hasPublicationInfo dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_assertion a np:Assertion .
  
  dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_provenance a np:Provenance .
  
  dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_assertion {
  miriam-gene:7422 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGNe249741e69ed57c9989e3184d937da78 sio:SIO_000628 miriam-gene:7422, lld:C1140680;
    a sio:SIO_001122 .
}

dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_provenance {
  dgn-np:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_assertion dcterms:description
      "[Findings from this study provide no evidence that rs3025033 and rs2146323 VEGF polymorphisms are associated with ovarian cancer survival. Although homozygous carriers of the tagSNP rs833068 experienced significantly worse survival in our Australian dataset, we were unable to replicate this in two independent datasets.]. 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:20832104;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP66917.RACnEB1lmeT27DkMInmrHMkp6LUZkGIUKpj0k9WntYPgs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}