@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs> .
@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:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_head {
  this: np:hasAssertion dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_assertion;
    np:hasProvenance dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_provenance;
    np:hasPublicationInfo dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_assertion a np:Assertion .
  
  dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_provenance a np:Provenance .
  
  dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0024623 a ncit:C7057 .
  
  dgn-gda:DGN4b3d35c3fdfd1a07580256d83dc57fe3 sio:SIO_000628 miriam-gene:2952, lld:C0024623;
    a sio:SIO_001122 .
}

dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_provenance {
  dgn-np:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_assertion dcterms:description
      "[Furthermore, the stomach cancer risk associated with the GSTT1 null genotype varied by age at diagnosis, with odds ratios of 3.85, 1.91, 1.78 and 0.59 for those diagnosed at ages less than 50, 50-59, 60-69 and 70 years or older, respectively (P trend = 0.01).]. 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:11692073;
    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:NP42816.RA2YXpxu3wwHrzbYG0srvYkcH_Tr32J19kT6USOQBM7gs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:19+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" .
}