@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY> .
@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:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_head {
  this: np:hasAssertion dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion ;
    np:hasProvenance dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_provenance ;
    np:hasPublicationInfo dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion a np:Assertion .
  dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_provenance a np:Provenance .
  dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion {
  miriam-gene:5444 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGN43db592d619fb65698f0c28a08e09ee0 sio:SIO_000628 miriam-gene:5444 , lld:C0020538 ;
    a sio:SIO_001122 .
}
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_provenance {
  dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion dcterms:description "[The finding that PON1192RR genotype is associated with$$$ a higher prevalence of arterial hypertension may contribute to improving the stratification of cardiovascular risk within a population aged 30-60 years. Determination of the PON1192 polymorphism may help to identify those individuals who are prone to developing cardiovascular diseases at an early stage, suggesting the need for close monitoring of cardiovascular risk factors before the onset of cardiovascular disease.]. 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:16794478 ;
    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:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:31+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" .
}