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Article

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

BMC bioinformatics - 5 Feb 2008

Furlong Laura I, Dach Holger, Hofmann-Apitius Martin, Sanz Ferran

Abstract excerpt

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...

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Identifiers

PMID: 18251998
DOI: 10.1186/1471-2105-9-84
PMCID: PMC2277400

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18251998-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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