@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U> .
@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:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_head {
  this: np:hasAssertion dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_assertion;
    np:hasProvenance dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_provenance;
    np:hasPublicationInfo dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_assertion a np:Assertion .
  
  dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_provenance a np:Provenance .
  
  dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_assertion {
  miriam-gene:2879 a ncit:C16612 .
  
  lld:C0038454 a ncit:C7057 .
  
  dgn-gda:DGN53231b6d402cdccfd34126cfb7bede81 sio:SIO_000628 miriam-gene:2879, lld:C0038454;
    a sio:SIO_001121 .
}

dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_provenance {
  dgn-np:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_assertion dcterms:description
      "[In the present study we have investigated the association of three single nucleotide polymorphisms in glutathione peroxidase (GPx) genes GPX1 rs1050450 (P198L), GPX3 rs2070593 (G930A) and GPX4 rs713041 (T718C) with the risk of cerebral stroke (CS) in patients with essential hypertension (EH).]. 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:22158110;
    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:NP551113.RAysidTzYnB9khqXEM1jtsxr7bx7mlcw5rDisQc-hzD3U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:32+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" .
}