ArticlePacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2006
PhenoGO: assigning phenotypic context to gene ontology annotations with natural language processing.
Article in Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
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Who cites it
29 citing papers in PubMed, 74 citations in OpenAlex.
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- A graph-based recovery and decomposition of Swanson's hypothesis using semantic predications.Journal of biomedical informatics · 2013Article
- Mining the pharmacogenomics literature--a survey of the state of the art.Briefings in bioinformatics · 2012Article
- An ontology-based comparative anatomy information system.Artificial intelligence in medicine · 2011Article
- Recent progress in automatically extracting information from the pharmacogenomic literature.Pharmacogenomics · 2010Review
- Molecular mechanistic associations of human diseases.BMC systems biology · 2010Article
- PhenoHM: human-mouse comparative phenome-genome server.Nucleic acids research · 2010Article
- MeSHing molecular sequences and clinical trials: a feasibility study.Journal of biomedical informatics · 2010Article
- Evaluation of an Ontology-anchored Natural Language-based Approach for Asserting Multi-scale Biomolecular Networks for Systems Medicine.Summit on translational bioinformatics · 2010Article
- Challenges for automatically extracting molecular interactions from full-text articles.BMC bioinformatics · 2009Article
- Integration of Neuroimaging and Microarray Datasets through Mapping and Model-Theoretic Semantic Decomposition of Unstructured Phenotypes.Cancer informatics · 2009Article
- Modeling and characterization of disease associated subnetworks in the human interactome using machine learning.Summit on translational bioinformatics · 2009Article
- Integration of Neuroimaging and Microarray Datasets through Mapping and Model-Theoretic Semantic Decomposition of Unstructured Phenotypes.Summit on translational bioinformatics · 2009Article
- PhenoGO: an integrated resource for the multiscale mining of clinical and biological data.BMC bioinformatics · 2009Article
- Mining clinical relationships from patient narratives.BMC bioinformatics · 2008Article
- E3Miner: a text mining tool for ubiquitin-protein ligases.Nucleic acids research · 2008Article
- Mining phenotypes for gene function prediction.BMC bioinformatics · 2008Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors at 1 institution in 1 country.
Funding
Abstract
Natural language processing (NLP) is a high throughput technology because it can process vast quantities of text within a reasonable time period. It has the potential to substantially facilitate biomedical research by extracting, linking, and organizing massive amounts of information that occur in biomedical journal articles as well as in textual fields of biological databases. Until recently, much of the work in biological NLP and text mining has revolved around recognizing the occurrence of biomolecular entities in articles, and in extracting particular relationships among the entities. Now, researchers have recognized a need to link the extracted information to ontologies or knowledge bases, which is a more difficult task. One such knowledge base is Gene Ontology annotations (GOA), which significantly increases semantic computations over the function, cellular components and processes of genes. For multicellular organisms, these annotations can be refined with phenotypic context, such as the cell type, tissue, and organ because establishing phenotypic contexts in which a gene is expressed is a crucial step for understanding the development and the molecular underpinning of the pathophysiology of diseases. In this paper, we propose a system, PhenoGO, which automatically augments annotations in GOA with additional context. PhenoGO utilizes an existing NLP system, called BioMedLEE, an existing knowledge-based phenotype organizer system (PhenOS) in conjunction with MeSH indexing and established biomedical ontologies. More specifically, PhenoGO adds phenotypic contextual information to existing associations between gene products and GO terms as specified in GOA. The system also maps the context to identifiers that are associated with different biomedical ontologies, including the UMLS, Cell Ontology, Mouse Anatomy, NCBI taxonomy, GO, and Mammalian Phenotype Ontology. In addition, PhenoGO was evaluated for coding of anatomical and cellular information and assigning the coded phenotypes to the correct GOA; results obtained show that PhenoGO has a precision of 91% and recall of 92%, demonstrating that the PhenoGO NLP system can accurately encode a large number of anatomical and cellular ontologies to GO annotations. The PhenoGO Database may be accessed at the following URL: http://www.phenoGO.org
Indexed as
Identifiers
17094228PMC2906243W2080007652What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.