OSIRISv1.2: A named entity recognition system for sequence variants of genes in biomedical literature

BACKGROUND: Single Nucleotide Polymorphisms, among other type of sequence variants, constitute key elements in genetic epidemiology and pharmacogenomics. While sequence data about genetic variation is found at databases such as dbSNP, clues about the functional and phenotypic consequences of the var...

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Detalles Bibliográficos
Autores principales: Furlong, Laura I, Dach, Holger, Hofmann-Apitius, Martin, Sanz, Ferran
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2277400/
https://www.ncbi.nlm.nih.gov/pubmed/18251998
http://dx.doi.org/10.1186/1471-2105-9-84

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2277400/
https://www.ncbi.nlm.nih.gov/pubmed/18251998
http://dx.doi.org/10.1186/1471-2105-9-84

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