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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 2010-07-13T09:31:29Z
dc.date.available 2010-07-13T09:31:29Z
dc.date.issued 2010-06
dc.identifier.citation Hastings, J, Dumontier, M, Hull, D. 2010. Representing chemicals using OWL, description graphs and rules. OWL: Experiences and Directions, 7th International Workshop. 21-22 June 2010, San Francisco, California, USA, pp 10 en
dc.identifier.uri http://hdl.handle.net/10204/4065
dc.description OWL: Experiences and Directions, 7th International Workshop. 21-22 June 2010, San Francisco, California, USA en
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 chemo informatics tools and applications, this internal structure is represented using chemical graphs. The authors here present a chemical knowledge base based on the standard chemical graph model using description graphs, OWL and rules. The authors include in our ontology chemical classes, groups, and molecules, together with their structures encoded as description graphs. They show how DL-safe rules can be used to determine parthood between groups and molecules based on the graph structures. Finally, they 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
dc.language.iso en en
dc.subject Ontology en
dc.subject Description graphs en
dc.subject Molecule parts en
dc.subject Graph structures en
dc.title Representing chemicals using OWL, description graphs and rules en
dc.type Conference Presentation en
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/10204/4065 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/10204/4065 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/10204/4065 . 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 chemo informatics tools and applications, this internal structure is represented using chemical graphs. The authors here present a chemical knowledge base based on the standard chemical graph model using description graphs, OWL and rules. The authors include in our ontology chemical classes, groups, and molecules, together with their structures encoded as description graphs. They show how DL-safe rules can be used to determine parthood between groups and molecules based on the graph structures. Finally, they 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 - Ontology KW - Description graphs KW - Molecule parts KW - Graph structures LK - https://researchspace.csir.co.za PY - 2010 T1 - Representing chemicals using OWL, description graphs and rules TI - Representing chemicals using OWL, description graphs and rules UR - http://hdl.handle.net/10204/4065 ER - en_ZA


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