@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI> .
@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/v3.0.0/void/> .
dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_head {
  this: np:hasAssertion dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_assertion ;
    np:hasProvenance dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_provenance ;
    np:hasPublicationInfo dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_assertion a np:Assertion .
  dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_provenance a np:Provenance .
  dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_assertion {
  miriam-gene:1557 a ncit:C16612 .
  lld:C0023895 a ncit:C7057 .
  dgn-gda:DGNfca7156c7b970829851b0529202fcc4b sio:SIO_000628 miriam-gene:1557 , lld:C0023895 ;
    a sio:SIO_001122 .
}
dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_provenance {
  dgn-np:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_assertion dcterms:description "[Frequencies of both CYP2C9 and CYP2C19 allelic variants, as well as CYP2D6 detrimental alleles, in Italian subjects were similar to those of other Caucasian populations. Conversely, the prevalence of CYP2D6 gene duplication among Italians resulted very hi]. 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:15177309 ;
    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:NP55015.RApgMRxGa5eONmVLUJHQX6JfhLAwGUXOBWV3nX2ed8rUI130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:10+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}