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The FAIR Guiding Principles for scientific data management and stewardship., , , , , , , , , and 6 other author(s). (2016)VarioML framework for comprehensive variation data representation and exchange., , , , , , , , , and 7 other author(s). BMC Bioinformatics, (2012)The FAIR Guiding Principles for scientific data management and stewardship, , , , , , , , , and 43 other author(s). Scientific Data, (March 2016)Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation., , , , , , , , and . Bioinformatics, 29 (16): 1997-2003 (2013)HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources., , , , , and . Nucleic Acids Research, 30 (1): 387-391 (2002)HGVbaseG2P: a central genetic association database., , , , , , , and . Nucleic Acids Research, 37 (Database-Issue): 797-802 (2009)HGVbase: a curated resource describing human DNA variation and phenotype relationships., , , , , , , and . Nucleic Acids Research, 32 (Database-Issue): 516-519 (2004)Extension to Distributed Annotation System: Summary command., , and . BHI, page 614-617. IEEE, (2014)G2P Knowledge Centre: An integrated genotype-phenotype data access portal and online collaborative network., and . IWBBIO, page 183. Copicentro Editorial, (2013)Semantically enabling a genome-wide association study database., , , and . J. Biomedical Semantics, (2012)