@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg> .
@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:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_head {
  this: np:hasAssertion dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion;
    np:hasProvenance dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_provenance;
    np:hasPublicationInfo dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion a np:Assertion .
  
  dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_provenance a np:Provenance .
  
  dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion {
  miriam-gene:1559 a ncit:C16612 .
  
  lld:C0013182 a ncit:C7057 .
  
  dgn-gda:DGN0cb37ec5625e9a0de8b20425cdbb0886 sio:SIO_000628 miriam-gene:1559, lld:C0013182;
    a sio:SIO_001122 .
}

dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_provenance {
  dgn-np:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_assertion dcterms:description
      "[This group of Inuit individuals are the first population in which no 2C9*2 or *3 alleles have been detected so far. Therefore, these alleles may be extremely rare or absent, and unless other novel polymorphisms exist in this Inuit group one would not anticipate any CYP2C9 poor metabolizer subjects among this population.]. 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:11697742;
    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:NP45748.RAOGrigpJT-qE-VSsrkIQM0SF2apk79K1nODRNGma4Izg130_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" .
}