@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc> .
@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:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_head {
  this: np:hasAssertion dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion ;
    np:hasProvenance dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_provenance ;
    np:hasPublicationInfo dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion a np:Assertion .
  dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_provenance a np:Provenance .
  dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion {
  miriam-gene:847 a ncit:C16612 .
  lld:C0020538 a ncit:C7057 .
  dgn-gda:DGNa729d84fdd93b776eec8ef791b5e68f3 sio:SIO_000628 miriam-gene:847 , lld:C0020538 ;
    a sio:SIO_001122 .
}
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_provenance {
  dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion dcterms:description "[Because chronic exposure to excess ROS may contribute to vascular damage, we investigated whether genetic variation in catalase was associated with susceptibility to essential hypertension (EHYT) in 324 individuals (at least 50 years old) who were randomly sampled from an isolated population living in Xiangchang, China.]. 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:11479740 ;
    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:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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 ;
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}