@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac> .
@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:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_head {
  this: np:hasAssertion dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_assertion;
    np:hasProvenance dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_provenance;
    np:hasPublicationInfo dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_assertion a np:Assertion .
  
  dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_provenance a np:Provenance .
  
  dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_assertion {
  miriam-gene:2690 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGNf67cb6f504e5cc9db3291059e1e6fe48 sio:SIO_000628 miriam-gene:2690, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_provenance {
  dgn-np:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_assertion dcterms:description
      "[Multivariate logistic regression analysis with adjustment for the same factors revealed that 11 polymorphisms in 11 genes (CAST, CTLA4, F5, GC, GHR, LIPC, PLA2G7, SLC4A1, SLCI8A1, TRH, VWF) showed significant associations with hypertension.]. 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:17137217;
    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:NP571970.RA--l-2lPxxWpxpRleLB5vQARpSBZMvbw6cvL2olT5zac130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:45+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" .
}