@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI> .
@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:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_head {
  this: np:hasAssertion dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion;
    np:hasProvenance dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_provenance;
    np:hasPublicationInfo dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion a np:Assertion .
  
  dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_provenance a np:Provenance .
  
  dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion {
  miriam-gene:10 a ncit:C16612 .
  
  lld:C0004096 a ncit:C7057 .
  
  dgn-gda:DGN73c7820289948eb56857d33dae65d311 sio:SIO_000628 miriam-gene:10, lld:C0004096;
    a sio:SIO_001122 .
}

dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_provenance {
  dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion dcterms:description
      "[Statistically significant increases in asthma risk were also observed among the whole study population for the concurrent presence of the GSTM1 null genotype and either NAT1 (odds ratio OR 4.53, 95% CI 1.76 to 11.6) or NAT2 (OR 3.12, 95% CI 1.11 to 8.78) slow acetylator genotypes, and of NAT1 and NAT2 slow acetylator genotypes (OR 4.20, 95% CI 1.51 to 11.6).]. 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:11927838;
    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:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}