Pages that link to "Q40695112"

The following pages link to Automatic extraction of mutations from Medline and cross-validation with OMIM. (Q40695112):

Displaying 47 items.

• Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers (Q21284327) (← links)
• An examination of the OMIM database for associating mutation to a consensus reference sequence (Q24658619) (← links)
• Facts from text--is text mining ready to deliver? (Q24804683) (← links)
• Getting personalized cancer genome analysis into the clinic: the challenges in bioinformatics (Q28394818) (← links)
• The HIV mutation browser: a resource for human immunodeficiency virus mutagenesis and polymorphism data (Q28542469) (← links)
• Benchmarking infrastructure for mutation text mining (Q28658315) (← links)
• Automatic extraction of protein point mutations using a graph bigram association. (Q30359637) (← links)
• A workflow for mutation extraction and structure annotation. (Q30366912) (← links)
• Improved mutation tagging with gene identifiers applied to membrane protein stability prediction (Q30380760) (← links)
• Interpretation of the consequences of mutations in protein kinases: combined use of bioinformatics and text mining (Q30422192) (← links)
• Toward an automatic method for extracting cancer- and other disease-related point mutations from the biomedical literature (Q30484760) (← links)
• MutationFinder: a high-performance system for extracting point mutation mentions from text (Q30831461) (← links)
• Gene-L'EXPO: a tool to extract knowledge From transcriptomes and find 'Literature-Sparse' relationships between genes and tissues. (Q30854141) (← links)
• The energy landscape analysis of cancer mutations in protein kinases (Q31038185) (← links)
• SYMBIOmatics: synergies in Medical Informatics and Bioinformatics--exploring current scientific literature for emerging topics (Q33281935) (← links)
• Deafness mutation mining using regular expression based pattern matching (Q33303929) (← links)
• Identification and analysis of co-occurrence networks with NetCutter. (Q33368056) (← links)
• Between proteins and phenotypes: annotation and interpretation of mutations (Q33503917) (← links)
• Extraction of human kinase mutations from literature, databases and genotyping studies (Q33503919) (← links)
• EnzyMiner: automatic identification of protein level mutations and their impact on target enzymes from PubMed abstracts (Q33503923) (← links)
• Annotation of protein residues based on a literature analysis: cross-validation against UniProtKb (Q33503926) (← links)
• Sequence and structure signatures of cancer mutation hotspots in protein kinases (Q33510934) (← links)
• Algorithms and semantic infrastructure for mutation impact extraction and grounding (Q33766739) (← links)
• Automated extraction and semantic analysis of mutation impacts from the biomedical literature (Q34324920) (← links)
• tmVar: a text mining approach for extracting sequence variants in biomedical literature (Q34657701) (← links)
• Text mining facilitates database curation - extraction of mutation-disease associations from Bio-medical literature (Q35654774) (← links)
• A Classification of Bioinformatics Algorithms from the Viewpoint of Maximizing Expected Accuracy (MEA) (Q35928874) (← links)
• DiMeX: A Text Mining System for Mutation-Disease Association Extraction. (Q35988105) (← links)
• Literature mining of protein-residue associations with graph rules learned through distant supervision (Q36300335) (← links)
• Medical informatics and bioinformatics: a bibliometric study. (Q36362179) (← links)
• Antisense oligonucleotides: from design to therapeutic application (Q36478849) (← links)
• OSIRISv1.2: a named entity recognition system for sequence variants of genes in biomedical literature (Q36514339) (← links)
• Towards precision medicine: advances in computational approaches for the analysis of human variants (Q37251907) (← links)
• The curation of genetic variants: difficulties and possible solutions (Q38073929) (← links)
• Structure-functional prediction and analysis of cancer mutation effects in protein kinases. (Q38987589) (← links)
• Towards a systematic evaluation of protein mutation extraction systems (Q40137414) (← links)
• Positional effects and strand preference of RNA interference against hepatitis C virus target sequences (Q40170241) (← links)
• Identification of universal selectivity-determining positions in cytochrome P450 monooxygenases by systematic sequence-based literature mining (Q40880012) (← links)
• Intrinsic evaluation of text mining tools may not predict performance on realistic tasks. (Q41887234) (← links)
• Prospects for the automated extraction of mutation data from the scientific literature (Q42331986) (← links)
• ABCMdb: A database for the comparative analysis of protein mutations in ABC transporters, and a potential framework for a general application (Q43417803) (← links)
• Application of automatic mutation-gene pair extraction to diseases (Q45780928) (← links)
• CoagMDB: a database analysis of missense mutations within four conserved domains in five vitamin K-dependent coagulation serine proteases using a text-mining tool (Q46866530) (← links)
• Identifying gene-specific variations in biomedical text (Q48075652) (← links)
• Retrieving mutation-specific information for human proteins in UniProt/Swiss-Prot Knowledgebase (Q48686540) (← links)
• Rapid pattern development for concept recognition systems: application to point mutations (Q51897382) (← links)
• MAGPEL: an autoMated pipeline for inferring vAriant-driven Gene PanEls from the full-length biomedical literature (Q97681241) (← links)