@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk> .
@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:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_head {
  this: np:hasAssertion dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion;
    np:hasProvenance dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_provenance;
    np:hasPublicationInfo dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion a np:Assertion .
  
  dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_provenance a np:Provenance .
  
  dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion {
  miriam-gene:196 a ncit:C16612 .
  
  lld:C0024299 a ncit:C7057 .
  
  dgn-gda:DGNb017c0828633ea6d20438ed72c7df85b sio:SIO_000628 miriam-gene:196, lld:C0024299;
    a sio:SIO_001122 .
}

dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_provenance {
  dgn-np:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_assertion dcterms:description
      "[In this case-control study conducted in British Columbia, Canada, five single nucleotide polymorphisms (SNPs) of AHR were genotyped in 422 NHL cases and 459 controls to measure the association between individual SNPs, haplotypes, and risk of NHL.]. 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:19821039;
    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:NP75244.RAGQYn9P-tLPr22lLwjIO5Iw0u6Layg-A_Fc_z281-YQk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:36+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" .
}