@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .
dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_head {
  this: np:hasAssertion dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_assertion ;
    np:hasProvenance dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_provenance ;
    np:hasPublicationInfo dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_assertion a np:Assertion .
  dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_provenance a np:Provenance .
  dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_assertion {
  miriam-gene:1559 a ncit:C16612 .
  lld:C0546837 a ncit:C7057 .
  dgn-gda:DGN82f5d36c66694688a1a5bff064e334fd sio:SIO_000628 miriam-gene:1559 , lld:C0546837 ;
    a sio:SIO_001122 .
}
dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_provenance {
  dgn-np:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_assertion dcterms:description "[ This is the first study to investigate a South American population for genetic polymorphism in the CYP2C subfamily. The Bolivian population differs from most other ethnic groups in the incidence of CYP2C9 and CYP2C19 common variants that might be influen]. 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:15776277 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP91358.RA3RKAMhp-WXoC7rSFpHQcMjYMV8gRZwHqfmV-1zz76F4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:29+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:disgenetv3.0rdf ;
    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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}