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Toward an automatic method for extracting cancer- and other disease-related point mutations from the biomedical literature

, , , , , , и . Bioinformatics, (2011)

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Session Introduction., , , , , и . PSB, стр. 507-511. (2018)Session Introduction., , , , , , и . Pacific Symposium on Biocomputing, стр. 228-230. World Scientific, (2008)Validating Candidate Gene-Mutation Relations in MEDLINE Abstracts via Crowdsourcing., , , , , , , , и . DILS, том 7348 из Lecture Notes in Computer Science, стр. 83-91. Springer, (2012)Session Introduction., , , , , и . Pacific Symposium on Biocomputing, стр. 464-466. (2009)Session Introduction., , , и . Pacific Symposium on Biocomputing, стр. 351-353. World Scientific, (2006)Oncodomains: A protein domain-centric framework for analyzing rare variants in tumor samples., , , , и . PLoS Comput. Biol., (2017)Detection of Encephalic and Hemorrhagic Viruses: Integration of Micro and Nano-fabrication with Computational Tools., , , , и . ICMENS, стр. 411-417. IEEE Computer Society, (2005)Incorporating molecular and functional context into the analysis and prioritization of human variants associated with cancer., , , и . JAMIA, 19 (2): 275-283 (2012)Session Introduction., , , и . Pacific Symposium on Biocomputing, стр. 1-3. World Scientific, (2007)Session introduction., , , , , , и . Pacific Symposium on Biocomputing, стр. 312-315. (2014)