@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ> .
@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 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:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_head {
  this: np:hasAssertion dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion;
    np:hasProvenance dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_provenance;
    np:hasPublicationInfo dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion a np:Assertion .
  
  dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_provenance a np:Provenance .
  
  dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion {
  miriam-gene:1576 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNf6f8fe3337870c2462fb20f5ed6236d3 sio:SIO_000628 miriam-gene:1576, lld:C0020538;
    a sio:SIO_001122 .
}

dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_provenance {
  dgn-np:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_assertion dct:description
      "[The CYP3A5 genotype was related with blood pressure in the general population, but the effect on the risk for hypertension in pregnancy has not been evaluated.We compared the allele and genotype frequencies of three functional SNPs in the CYP3A5 (rs776746), CYP3A4 (rs2740574), and CYP21A2 (rs6471) genes between pregnant women who developed hypertension (n = 250) or who remained normotensive (control group, n = 250).]. 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:20617557;
    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:NP60075.RA-fwxZUiWqFFkgDds_8buvvB5r2hnOLuSCLbKggtq6wQ130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}