@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI> .
@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:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_head {
  this: np:hasAssertion dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion;
    np:hasProvenance dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_provenance;
    np:hasPublicationInfo dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion a np:Assertion .
  
  dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_provenance a np:Provenance .
  
  dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion {
  miriam-gene:574045 a ncit:C16612 .
  
  lld:C0011849 a ncit:C7057 .
  
  dgn-gda:DGN6a02434d72fde9ddb14bf583da746ecd sio:SIO_000628 miriam-gene:574045, lld:C0011849;
    a sio:SIO_001121 .
}

dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_provenance {
  dgn-np:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_assertion dcterms:description
      "[A total of 155 Hispanic living kidney donors as controls and a total of 86 Hispanic kidney transplant patients, whose renal failure was attributed to hypertensive nephropathy after ruling out diabetes mellitus or other causes, were genotyped for four different single nucleotide polymorphisms of VEGF: -2578 C>A (rs699947), -1154 G>A (rs1570360), -460 C>T (rs833061), and +936 C>T (rs3025039).]. 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:21080079;
    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:NP411344.RAq3cN-fmSRtKCAzm_jHbFOcORyObjnkTFpUiYpDJ08NI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:04+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" .
}