@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0> .
@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:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_head {
  this: np:hasAssertion dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion;
    np:hasProvenance dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_provenance;
    np:hasPublicationInfo dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion a np:Assertion .
  
  dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_provenance a np:Provenance .
  
  dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0026764 a ncit:C7057 .
  
  dgn-gda:DGN1742ec0f5e91961f38706ebb9d3c3733 sio:SIO_000628 miriam-gene:1543, lld:C0026764;
    a sio:SIO_001122 .
}

dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_provenance {
  dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion dcterms:description
      "[In a case-control study, 90 Australian Caucasians with MM had significantly higher incidences of GST T1 null, PON1 BB and NAT2 slow acetylation genotypes, but no difference in polymorphism frequencies for GST M1, NAT1, and CYP1A1 when compared to 205 controls.]. 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:15136237;
    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:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_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;
    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" .
}