@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc> .
@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:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_head {
  this: np:hasAssertion dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_assertion;
    np:hasProvenance dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_provenance;
    np:hasPublicationInfo dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_assertion a np:Assertion .
  
  dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_provenance a np:Provenance .
  
  dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0020538 a ncit:C7057 .
  
  dgn-gda:DGN549ef525b9db4d69cf3babd942623aa9 sio:SIO_000628 miriam-gene:2944, lld:C0020538;
    a sio:SIO_001121 .
}

dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_provenance {
  dgn-np:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_assertion dcterms:description
      "[We then genotyped 753 trios from the Medical Research Council British Genetics of Hypertension Study transmission disequilibrium test cohort for 10 single nucleotide polymorphisms and the GSTM1 deletion and examined renal GSTM expression in a cohort of 27 hypertensive and 18 normotensive subjects.]. 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:18551009;
    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:NP561281.RAcTsM3SgkFJt0iXeoEH5TVaQTgOTo9tZjjVkgYhqZfgc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:38+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" .
}