Abstract
We present in this paper the architecture and some implementation details of a Document Management System and Workflow to help in the diagnosis of the hypertrophic cardiomyopathy, one of the most frequent genetic cardiovascular diseases. The system allows a gradual and collaborative creation of a knowledge base about the mutations associated with this disease. The system manages both the original documents of the scientific papers and the data extracted from these papers by the experts. Furthermore, a semiautomatic report generation module exploits this knowledge base to create high quality reports about the studied mutations.
This work has been partially supported by “Centro para el desarrollo tecnológico industrial (CDTI) del Ministerio de Industria” ref. Neotec RD 1406/1986 (IDI “20070178”, title “Plataforma de diagnóstico genético de Cardiopatías”) and by “Xunta de Galicia” ref. 08SIN008E. Other institutions collaborating in the support of the researchers are “Ministerio de Educación y Ciencia” (PGE y FEDER) ref. TIN2006-15071-C03-03 and “Xunta de Galicia” ref. 2006/4.
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Montserrat, L., Cotelo-Lema, J.A., Luaces, M.R., Seco, D. (2010). Collecting, Analyzing, and Publishing Massive Data about the Hypertrophic Cardiomyopathy. In: Fred, A., Filipe, J., Gamboa, H. (eds) Biomedical Engineering Systems and Technologies. BIOSTEC 2009. Communications in Computer and Information Science, vol 52. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-11721-3_23
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DOI: https://doi.org/10.1007/978-3-642-11721-3_23
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