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PGxO

A lightweight and simple ontology to reconcile and trace knowledge in pharmacogenomics (PGx).

PGxO is also available on the NCBO BioPortal.

A full description of the motivation, implementation and instantiation of PGxO is available in [2].

When citing PGxO, please use [2].

Documentation

Documentation is available in the doc/ folder:

Mappings

Mappings are available in the mappings/ folder:

  • mapp1.owl: Mappings from PGxO to four ontologies related to PGx (SO-PHARM, PO, PHARE and Genomic CDS).
  • mapp2.owl: Mappings from PGxO to three large spectrum ontologies (MeSH, NCIt and SNOMED CT).

License

PGxO is under Creative Commons BY NC 4.0.

References

  1. Monnin, P., Jonquet, C., Legrand, J., Napoli, A., & Coulet, A. (2017, October). PGxO: A very lite ontology to reconcile pharmacogenomic knowledge units. In Methods, tools & platforms for Personalized Medicine in the Big Data Era. Link
  2. Monnin, P., Legrand, J., Husson, G., Ringot, P., Tchechmedjiev, A., Jonquet, C., Napoli, A., & Coulet, A. PGxO and PGxLOD: a reconciliation of pharmacogenomic knowledge of various provenances, enabling further comparison. BMC Bioinformatics 20-S(4): 139:1-139:16 (2019). Link
@Article{Monnin2019, author="Monnin, Pierre and Legrand, Jo{\"e}l and Husson, Graziella and Ringot, Patrice and Tchechmedjiev, Andon and Jonquet, Cl{\'e}ment and Napoli, Amedeo and Coulet, Adrien", title="PGxO and PGxLOD: a reconciliation of pharmacogenomic knowledge of various provenances, enabling further comparison", journal="BMC Bioinformatics", year="2019", month="Apr", day="18", volume="20-S", number="4", pages="139", issn="1471-2105", doi="10.1186/s12859-019-2693-9", url="https://doi.org/10.1186/s12859-019-2693-9" } 

Acknowledgments

PGxO is supported by the PractiKPharma project (http://practikpharma.loria.fr/), funded by the French National Research Agency (ANR) under grant ANR-15-CE23-0028.

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A lightweight and simple ontology to reconcile and trace knowledge in pharmacogenomics

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