@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg> .
@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:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_head {
  this: np:hasAssertion dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_assertion;
    np:hasProvenance dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_provenance;
    np:hasPublicationInfo dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_assertion a np:Assertion .
  
  dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_provenance a np:Provenance .
  
  dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_assertion {
  miriam-gene:196 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
  dgn-gda:DGN30d40fecc479ec0493af8699bf6b5733 sio:SIO_000628 miriam-gene:196, lld:C0005684;
    a sio:SIO_001122 .
}

dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_provenance {
  dgn-np:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_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: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:NP48751.RA-66XtRPSHJr5z4u8s3KVFyItVG9_PImlF4zvpRhNGMg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:22+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" .
}