@prefix dc: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix eco: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP84026.RAQ7IVqeu00hI6aFJ2fOkmGIx8VqL0R31TCf0gXi5kPQ8130_head {
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dgn-np:NP84026.RAQ7IVqeu00hI6aFJ2fOkmGIx8VqL0R31TCf0gXi5kPQ8130_assertion {
miriam-gene:9429 a ncit:C16612 .
lld:C0023474 a ncit:C7057 .
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dgn-np:NP84026.RAQ7IVqeu00hI6aFJ2fOkmGIx8VqL0R31TCf0gXi5kPQ8130_provenance {
dgn-np:NP84026.RAQ7IVqeu00hI6aFJ2fOkmGIx8VqL0R31TCf0gXi5kPQ8130_assertion dc:description
"[In this study, associations between IM trough concentration, clinical response and 11 single-nucleotide polymorphisms in genes involved in IM pharmacokinetics (ABCB1, ABCC2, ABCG2 CYP3A5, SLC22A1 and SLCO1B3) were investigated among 67 Japanese chronic phase CML patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
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sio:SIO_000772 miriam-pubmed:20720558;
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rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
rdfs:label "DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP84026.RAQ7IVqeu00hI6aFJ2fOkmGIx8VqL0R31TCf0gXi5kPQ8130_publicationInfo {
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dc:rights ;
dc:rightsHolder dgn-void:IBIGroup;
dc:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetrdf;
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, , ;
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