@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE> .
@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:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_head {
   this: np:hasAssertion dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_assertion ;
    np:hasProvenance dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_provenance ;
    np:hasPublicationInfo dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_assertion a np:Assertion .
  dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_provenance a np:Provenance .
  dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_assertion {
   miriam-gene:7200 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGNd70004e3a816ee8831a10aaa7102ab2c sio:SIO_000628 miriam-gene:7200 , lld:C0020538 ;
    a sio:SIO_001121 .
}
dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_provenance {
   dgn-np:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_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:NP726085.RAtPMT-mFhzdh_M1cf9Ai1KXni5-jOginBLxorRC3U7FE130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:20+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" .
}