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Representing chemicals using OWL, description graphs and rules

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dc.contributor.author Hastings, J
dc.contributor.author Dumontier, M
dc.contributor.author Hull, D
dc.contributor.author Horridge, M
dc.contributor.author Steinbeck, C
dc.contributor.author Sattler, U
dc.contributor.author Stevens, R
dc.contributor.author Horne, T
dc.contributor.author Britz, K
dc.date.accessioned 2011-03-28T07:59:10Z
dc.date.available 2011-03-28T07:59:10Z
dc.date.issued 2010-06
dc.identifier.citation Hastings, J, Dumontier, M, Hull D et al. 2010. Representing chemicals using OWL, description graphs and rules. OWL: experiences and directions, OWLED 2010: 7th International Workshop, San Francisco, California, USA, 21-22 June 2010, pp 10 en_US
dc.identifier.issn 1613-0073
dc.identifier.uri http://krr.meraka.org.za/wp-content/uploads/2010/07/owled_descgraphschem_2010.pdf
dc.identifier.uri http://hdl.handle.net/10204/4919
dc.description 7th International Workshop, San Francisco, California, USA, 21-22 June 2010 en_US
dc.description.abstract Objects can be said to be structured when their representation also contains their parts. While OWL in general can describe structured objects, description graphs are a recent, decidable extension to OWL which support the description of classes of structured objects whose parts are related in complex ways. Classes of chemical entities such as molecules, ions and groups (parts of molecules) are often characterised by the way in which the constituent atoms of their instances are connected via chemical bonds. For chemoinformatics tools and applications, this internal structure is represented using chemical graphs. We here present a chemical knowledge base based on the standard chemical graph model using description graphs, OWL and rules. We include in our ontology chemical classes, groups, and molecules, together with their structures encoded as description graphs. We show how DL-safe rules can be used to determine parthood between groups and molecules based on the graph structures. Finally, we investigate the scalability of the technology used through the development of an automatic utility to convert standard chemical graphs into description graphs, and converting a large number of diverse graphs obtained from a publicly available chemical database. en_US
dc.language.iso en en_US
dc.relation.ispartofseries Workflow;6073
dc.subject Chemicals en_US
dc.subject Ontology en_US
dc.subject Description graphs en_US
dc.subject OWL en_US
dc.subject Molecule parts en_US
dc.subject Graph structures en_US
dc.subject Structured objects en_US
dc.title Representing chemicals using OWL, description graphs and rules en_US
dc.type Conference Presentation en_US
dc.identifier.apacitation Hastings, J., Dumontier, M., Hull, D., Horridge, M., Steinbeck, C., Sattler, U., ... Britz, K. (2010). Representing chemicals using OWL, description graphs and rules. http://hdl.handle.net/10204/4919 en_ZA
dc.identifier.chicagocitation Hastings, J, M Dumontier, D Hull, M Horridge, C Steinbeck, U Sattler, R Stevens, T Horne, and K Britz. "Representing chemicals using OWL, description graphs and rules." (2010): http://hdl.handle.net/10204/4919 en_ZA
dc.identifier.vancouvercitation Hastings J, Dumontier M, Hull D, Horridge M, Steinbeck C, Sattler U, et al, Representing chemicals using OWL, description graphs and rules; 2010. http://hdl.handle.net/10204/4919 . en_ZA
dc.identifier.ris TY - Conference Presentation AU - Hastings, J AU - Dumontier, M AU - Hull, D AU - Horridge, M AU - Steinbeck, C AU - Sattler, U AU - Stevens, R AU - Horne, T AU - Britz, K AB - Objects can be said to be structured when their representation also contains their parts. While OWL in general can describe structured objects, description graphs are a recent, decidable extension to OWL which support the description of classes of structured objects whose parts are related in complex ways. Classes of chemical entities such as molecules, ions and groups (parts of molecules) are often characterised by the way in which the constituent atoms of their instances are connected via chemical bonds. For chemoinformatics tools and applications, this internal structure is represented using chemical graphs. We here present a chemical knowledge base based on the standard chemical graph model using description graphs, OWL and rules. We include in our ontology chemical classes, groups, and molecules, together with their structures encoded as description graphs. We show how DL-safe rules can be used to determine parthood between groups and molecules based on the graph structures. Finally, we investigate the scalability of the technology used through the development of an automatic utility to convert standard chemical graphs into description graphs, and converting a large number of diverse graphs obtained from a publicly available chemical database. DA - 2010-06 DB - ResearchSpace DP - CSIR KW - Chemicals KW - Ontology KW - Description graphs KW - OWL KW - Molecule parts KW - Graph structures KW - Structured objects LK - https://researchspace.csir.co.za PY - 2010 SM - 1613-0073 T1 - Representing chemicals using OWL, description graphs and rules TI - Representing chemicals using OWL, description graphs and rules UR - http://hdl.handle.net/10204/4919 ER - en_ZA


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