@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0> .
@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:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_head {
  this: np:hasAssertion dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_assertion;
    np:hasProvenance dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_provenance;
    np:hasPublicationInfo dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_assertion a np:Assertion .
  
  dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_provenance a np:Provenance .
  
  dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_assertion {
  miriam-gene:7941 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_provenance {
  dgn-np:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_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;
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    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:NP913938.RAd78xklstmuYvcDAkZ5OCkApyrr8YB52rzzvRkZCMvd0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:21+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>,
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}