@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0> .
@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:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_head {
  this: np:hasAssertion dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion;
    np:hasProvenance dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_provenance;
    np:hasPublicationInfo dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion a np:Assertion .
  
  dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_provenance a np:Provenance .
  
  dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion {
  miriam-gene:7422 a ncit:C16612 .
  
  lld:C0948089 a ncit:C7057 .
  
  dgn-gda:DGN0dcf7dc94b648650e0f61a2fbc298d3f sio:SIO_000628 miriam-gene:7422, lld:C0948089;
    a sio:SIO_001121 .
}

dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_provenance {
  dgn-np:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_assertion dcterms:description
      "[Several common polymorphisms in the promoter region of the VEGF gene have been reported, but only few single nucleotide polymorphisms (SNPs) have been demonstrated to be associated with variations in VEGF serum concentrations and with a susceptibility to CAD and its complications-acute coronary syndromes.]. 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:20210775;
    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:NP792672.RAaRV6TFarEfh_g61CGLQw01TTKxEyGd9gL4nPvWFWmv0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:06+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" .
}