2012
DOI: 10.1186/1471-2105-13-s1-s7
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Transparent mediation-based access to multiple yeast data sources using an ontology driven interface

Abstract: BackgroundSaccharomyces cerevisiae is recognized as a model system representing a simple eukaryote whose genome can be easily manipulated. Information solicited by scientists on its biological entities (Proteins, Genes, RNAs...) is scattered within several data sources like SGD, Yeastract, CYGD-MIPS, BioGrid, PhosphoGrid, etc. Because of the heterogeneity of these sources, querying them separately and then manually combining the returned results is a complex and time-consuming task for biologists most of whom … Show more

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Cited by 6 publications
(4 citation statements)
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“…Comments, corrections and/or clarifications regarding PhosphoGRID can be sent to admin@phosphogrid.org. Since its introduction in 2010, PhosphoGRID has become one of the five most visited online databases by the Saccharomyces research community, along with SGD (6), Yeastract (7), CYGD-MIPS (8) and BioGRID (9). …”
Section: Introductionmentioning
confidence: 99%
“…Comments, corrections and/or clarifications regarding PhosphoGRID can be sent to admin@phosphogrid.org. Since its introduction in 2010, PhosphoGRID has become one of the five most visited online databases by the Saccharomyces research community, along with SGD (6), Yeastract (7), CYGD-MIPS (8) and BioGRID (9). …”
Section: Introductionmentioning
confidence: 99%
“…It uses various technologies for developing Web applications such as SOAP/XML, WSDL, UDDI, XSDL, RDF, and DAML+ OIL. YeastMed 36 is a mediator‐based system for the integration of yeast‐specific data sources such as SGD, YEASTRACT, MIPS‐CYGD, BioGRID, and PhosphoGRID. It has a domain ontology that plays the role of the global schema and supports the user queries.…”
Section: Related Workmentioning
confidence: 99%
“…"Towards Linked Open Gene Mutations Data" by Zappa et al . [ 9 ] presents a prototype implementation of the IARC TP53 Mutation database as Linked Open Data (LOD) that allows to semantically integrate mutation data with information from public molecular biology databases whose content is already available through the LOD and can also serve as a starting point for the development of an ontology on human variation data.…”
Section: Prefacementioning
confidence: 99%