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J Biomed Inform. 2013 Aug;46(4):690-6. doi: 10.1016/j.jbi.2013.05.005. Epub 2013 May 29.

Disambiguation of PharmGKB drug-disease relations with NDF-RT and SPL.

Author information

1
Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA. zhu.qian@mayo.edu

Abstract

PharmGKB is a leading resource of high quality pharmacogenomics data that provides information about how genetic variations modulate an individual's response to drugs. PharmGKB contains information about genetic variations, pharmacokinetic and pharmacodynamic pathways, and the effect of variations on drug-related phenotypes. These relationships are represented using very general terms, however, and the precise semantic relationships among drugs, and diseases are not often captured. In this paper we develop a protocol to detect and disambiguate general clinical associations between drugs and diseases using more precise annotation terms from other data sources. PharmGKB provides very detailed clinical associations between genetic variants and drug response, including genotype-specific drug dosing guidelines, and this procedure will armGKB. The availability of more detailed data will help investigators to conduct more precise queries, such as finding particular diseases caused or treated by a specific drug. We first mapped drugs extracted from PharmGKB drug-disease relationships to those in the National Drug File Reference Terminology (NDF-RT) and to Structured Product Labels (SPLs). Specifically, we retrieved drug and disease role relationships describing and defining concepts according to their relationships with other concepts from NDF-RT. We also used the NCBO (National Center for Biomedical Ontology) annotator to annotate disease terms from the free text extracted from five SPL sections (indication, contraindication, ADE, precaution, and warning). Finally, we used the detailed drug and disease relationship information from NDF-RT and the SPLs to annotate and disambiguate the more general PharmGKB drug and disease associations.

KEYWORDS:

Clinical associations; NDF-RT; PharmGKB; Pharmacogenomics; SPL

PMID:
23727027
PMCID:
PMC3746070
DOI:
10.1016/j.jbi.2013.05.005
[Indexed for MEDLINE]
Free PMC Article
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