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Paper Details

The de novo FAIRification process of a registry for vascular anomalies.
Orphanet J Rare Dis
8
2021
Common, Patient, Rare Disease, humans, rare, rare disease, vascular anomalies
Author NameAffiliation
Rajaram KaliyaperumalLeiden University Medical Center
Peter A C 't HoenCenter for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center
Peter A C 't HoenCenter for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center
Ronald CornetAmsterdam Public Health Research Institute, University of Amsterdam
Marco RoosLeiden University Medical Center
Marco RoosLeiden University Medical Center
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