DiMeX: A Text Mining System for Mutation-Disease Association Extraction

tmVar: a text mining approach for extracting sequence variants in biomedical literature

(2013) C.-H. Wei et al.   BIOINFORMATICS

The InSiGHT database: utilizing 100 years of insights into Lynch Syndrome

(2013) J. P. Plazzer et al.   Familial Cancer

Activities at the Universal Protein Resource (UniProt)

(2013)   NUCLEIC ACIDS RESEARCH

PubTator: a web-based text mining tool for assisting biocuration

(2013) Chih-Hsuan Wei et al.   NUCLEIC ACIDS RESEARCH

ClinVar: public archive of relationships among sequence variation and human phenotype

(2013) Melissa J. Landrum et al.   NUCLEIC ACIDS RESEARCH

Automatic recognition of conceptualization zones in scientific articles and two life science applications

(2012) Maria Liakata et al.   BIOINFORMATICS

Extracting semantically enriched events from biomedical literature

(2012) Makoto Miwa et al.   BMC BIOINFORMATICS

Automated extraction and semantic analysis of mutation impacts from the biomedical literature

(2012) Nona Naderi et al.   BMC GENOMICS

Bioinformatics for personal genome interpretation

(2012) E. Capriotti et al.   BRIEFINGS IN BIOINFORMATICS

Pharmacogenomics Knowledge for Personalized Medicine

(2012) M Whirl-Carrillo et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

Enriching a biomedical event corpus with meta-knowledge annotation

(2011) Paul Thompson et al.   BMC BIOINFORMATICS

Automatic classification of sentences to support Evidence Based Medicine

(2011) Su Kim et al.   BMC BIOINFORMATICS

Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers

(2011) Philippe E Thomas et al.   BMC BIOINFORMATICS

The impact of next-generation sequencing on genomics

(2011) Jun Zhang et al.   Journal of Genetics and Genomics

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

(2010) Emily Doughty et al.   BIOINFORMATICS

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

(2010) S. A. Forbes et al.   NUCLEIC ACIDS RESEARCH

Improved mutation tagging with gene identifiers applied to membrane protein stability prediction

(2009) Rainer Winnenburg et al.   BMC BIOINFORMATICS

EnzyMiner: automatic identification of protein level mutations and their impact on target enzymes from PubMed abstracts

(2009) Süveyda Yeniterzi et al.   BMC BIOINFORMATICS

The Human Gene Mutation Database: 2008 update

(2009) Peter D Stenson et al.   Genome Medicine

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

(2008) Laura I Furlong et al.   BMC BIOINFORMATICS

PolySearch: a web-based text mining system for extracting relationships between human diseases, genes, mutations, drugs and metabolites

(2008) D. Cheng et al.   NUCLEIC ACIDS RESEARCH

HGVbaseG2P: a central genetic association database

(2008) G. A. Thorisson et al.   NUCLEIC ACIDS RESEARCH

McKusick's Online Mendelian Inheritance in Man (OMIM(R))

(2008) J. Amberger et al.   NUCLEIC ACIDS RESEARCH

CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool

(2007) Rebecca E. Saunders et al.   HUMAN MUTATION