Mapping of the dataset of the German National Regsitry for Rare Diseases (NARSE) to Observational Medical Outcomes Partnership Common Data Model (OMOP CDM)
收藏Zenodo2024-05-03 更新2026-05-26 收录
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https://zenodo.org/doi/10.5281/zenodo.11072076
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Mapping between the data set of the German National Registry for Rare Diseases ("Nationales Register für Seltene Erkrankungen"; NARSE) to Observational Medical Outcomes Partnership Common Data Model (OMOP CDM) using international standards.
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Zenodo创建时间：
2024-04-29
