@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc> .
@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:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_head {
  this: np:hasAssertion dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_assertion ;
    np:hasProvenance dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_provenance ;
    np:hasPublicationInfo dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_assertion a np:Assertion .
  dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_provenance a np:Provenance .
  dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_assertion {
  miriam-gene:1577 a ncit:C16612 .
  lld:C0023473 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_provenance {
  dgn-np:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_assertion dcterms:description "[This study explored the association of 14 single nucleotide polymorphisms in three genes coding for influx transporters (SLC22A1, SLCO1B1, and SLCO1B3), two genes coding for efflux transporters (ABCB1 and ABCG2), and four genes coding for enzymes (CYP2C9, CYP2C19, CYP2D6, and CYP3A5) with the pharmacokinetics of imatinib in Japanese patients with chronic myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP855398.RA5KWH6aFmxcOiaHeuU8KSVPpaZSNEYphOMsrSD9Ngzjc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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 ;
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}