@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno> .
@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 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:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_head {
  this: np:hasAssertion dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_assertion ;
    np:hasProvenance dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_provenance ;
    np:hasPublicationInfo dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_assertion a np:Assertion .
  dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_provenance a np:Provenance .
  dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_assertion {
  miriam-gene:847 a ncit:C16612 .
  lld:C0085580 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_provenance {
  dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_assertion dc: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 ;
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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 ;
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}
dgn-np:NP377731.RACG_J-n7HCOWLadRKw_UrH226DplZo4vKlA8gz8bnAno130_publicationInfo {
  this: dc:created "2014-10-02T12:35:41+02:00"^^xsd:dateTime ;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dc:rightsHolder dgn-void:IBIGroup ;
    dc:subject sio:SIO_000983 ;
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