@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o> .
@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:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_head {
  this: np:hasAssertion dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_assertion;
    np:hasProvenance dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_provenance;
    np:hasPublicationInfo dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_assertion a np:Assertion .
  
  dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_provenance a np:Provenance .
  
  dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_assertion {
  miriam-gene:196 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
  dgn-gda:DGNab305e3ef817fa619880266659de9498 sio:SIO_000628 miriam-gene:196, lld:C0005684;
    a sio:SIO_001121 .
}

dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_provenance {
  dgn-np:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_assertion dcterms:description
      "[To assess two polymorphic forms of aryl hydrocarbon receptor (AHR) gene, G1721A (R554K), and G1768A (V570I) in Chinese population and to explore the possible association of human AHR gene polymorphism with elevated incidence of bladder cancer among Chinese Han subjects in east of China.]. 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:11866883;
    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:NP298588.RAm3VAaGQ9rehbcwKWV18i-0iORCp92MWfGMkiUomYk1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:49+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" .
}