@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164> .
@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:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_head {
   this: np:hasAssertion dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_assertion ;
    np:hasProvenance dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_provenance ;
    np:hasPublicationInfo dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_assertion a np:Assertion .
  dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_provenance a np:Provenance .
  dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_assertion {
   miriam-gene:26059 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN005401ed8b7556c6d6efac00db211001 sio:SIO_000628 miriam-gene:26059 , lld:C0020538 ;
    a sio:SIO_001121 .
}
dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_provenance {
   dgn-np:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_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:NP623719.RAILYTlNtF_tMSwdUiu2nn17VX7_04fjD4EBEM2qat164130_publicationInfo {
   this: dcterms:created "2014-10-02T12:38:16+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" .
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}