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http://archive.gramene.org/plant_ontology/ontology_browse.html#to
A controlled vocabulary to describe phenotypic traits in plants. Each trait is a distinguishable feature, characteristic, quality or phenotypic feature of a developing or mature plant, or a plant part.
Proper citation: Plant Trait Ontology (RRID:SCR_003461) Copy
http://www.loria.fr/~coulet/sopharm2.0_description.php
A domain ontology implemented in OWL-DL, which proposes a formal description of pharmacogenomic knowledge. It articulates different ontologies that represent complementary sub-domains of pharmacogenomics, i.e. related to genotype, phenotype, drugs, and clinical trials. SO-Pharm enables the representation of pharmacogenomic relationships between a drug, a genomic variation and a phenotype trait. In addition, it enables the representation of a patient and more largely a panel included in trials, and populations. SO-Pharm enables the representation of measured items on patients such as results from the observation of a phenotype trait or of genomic variations. SO-Pharm supports knowledge about pharmacogenomic hypothesis, case study, and investigations in pharmacogenomics. SO-Pharm is designed to facilitate data integration and knowledge discovery in pharmacogenomics. In addition it provides a consistent articulation of ontologies of pharmacogenomic sub-domains.
Proper citation: Suggested Ontology for Pharmacogenomics (RRID:SCR_003497) Copy
An ontology of physico-chemical processes, i.e. physico-chemical changes occurring in course of time. It includes both microscopic processes (involving molecular entities or subatomic particles) and macroscopic processes. Some biochemical processes from Gene Ontology (GO Biological process) can be described as instances of REX.
Proper citation: Physico-Chemical Process (RRID:SCR_003530) Copy
An ontology for describing software tools, their types, tasks, versions, provenance and data associated (the input and output data types and the uses the software can be put to).
Proper citation: Software Ontology (RRID:SCR_003493) Copy
Ontology that describes structures from the dimensional range encompassing cellular and subcellular structure, supracellular domains, and macromolecules. It is built according to ontology development best practices (re-use of existing ontologies; formal definitions of terms; use of foundational ontologies). It describes the parts of neurons and glia and how these parts come together to define supracellular structures such as synapses and neuropil. Molecular specializations of each compartment and cell type are identified. The SAO was designed with the goal of providing a means to annotate cellular and subcellular data obtained from light and electron microscopy, including assigning macromolecules to their appropriate subcellular domains. The SAO thus provides a bridge between ontologies that describe molecular species and those concerned with more gross anatomical scales. Because it is intended to integrate into ontological efforts at these other scales, particular care was taken to construct the ontology in a way that supports such integration.
Proper citation: Subcellular Anatomy Ontology (RRID:SCR_003486) Copy
http://purl.bioontology.org/ontology/VTO
An ontology that includes both extinct and extant vertebrates, aiming to provide one comprehensive hierarchy. The hierarchy backbone for extant taxa is based on the NCBI taxonomy. Since the NCBI taxonomy only includes species associated with archived genetic data, to complement this, they also incorporate taxonomic information across the vertebrates from the Paleobiology Database (PaleoDB). The Teleost Taxonomy Ontology (TTO) and AmphibiaWeb (AWeb) are incorporated to provide a more authoritative hierarchy and a richer set of names for specific taxonomic groups.
Proper citation: Vertebrate Taxonomy Ontology (RRID:SCR_003518) Copy
http://purl.bioontology.org/ontology/ICPS
Ontology network about Patient Safety Incident. This work has been carried out by the Ontological Engineering Group, using sources from the University of Saint Etienne and the Australian Patient Safety Foundation.
Proper citation: International Classification for Patient Safety (RRID:SCR_003553) Copy
http://purl.bioontology.org/ontology/MDDB
Ontology of master drug data base, 2009_08_05
Proper citation: Master Drug Data Base Clinical Drugs (RRID:SCR_003668) Copy
https://bioportal.bioontology.org/ontologies/NEMO/?p=summary
Ontology that describes classes of event-related brain potentials (ERP) and their properties, including spatial, temporal, and functional (cognitive / behavioral) attributes, and data-level attributes (acquisition and analysis parameters). Its aim is to support data sharing, logic-based queries and mapping/integration of patterns across data from different labs, experiment paradigms, and modalities (EEG/MEG).
Proper citation: NEMO Ontology (RRID:SCR_003386) Copy
http://purl.bioontology.org/ontology/MSTDE
Metathesaurus Version of Minimal Standard Terminology Digestive Endoscopy. Bethesda, MD: National Library of Medicine, 2001.
Proper citation: Minimal Standard Terminology of Digestive Endoscopy (RRID:SCR_003785) Copy
http://purl.bioontology.org/ontology/SNMI
Ontology of systematized nomenclature of human and veterinary medicine: SNOMED International. Cote, Roger A., editor. Northfield (IL): College of American Pathologists; Schaumburg (IL): American Veterinary Medical Association, Version 3.5, 1998.
Proper citation: Systematized Nomenclature of Medicine - International Version (RRID:SCR_003849) Copy
http://purl.bioontology.org/ontology/MFO
A structured controlled vocabulary of the anatomy and development of the Japanese medaka fish, Oryzias latipes.
Proper citation: Medaka Fish Anatomy and Development Ontology (RRID:SCR_003719) Copy
http://purl.bioontology.org/ontology/NIGO
Ontology that is a subset of GO directed for neurological and immunological systems. It was created by clipping those GO terms that are not associated to any gene in human, rat and mouse, and by clipping terms not found to be relevant to the neural and/or immune domains.
Proper citation: Neural-Immune Gene Ontology (RRID:SCR_004120) Copy
http://code.google.com/p/eagle-i/
Ontology that models research resources such as instruments, protocols, reagents, animal models and biospecimens. It has been developed in the context of the eagle-i project (http://eagle-i.net/) and consists of over 3451 classes of which over 1200 were created within the ERO namespace, while the rest come from existent ontologies such as the Ontology for Biomedical Investigation (OBI), the uber-anatomy ontology (Uberon), VIVO, the Ontology for Clinical Research (OCRe), the Sequence Ontology (SO), the Software Ontology (SWO) and we include terms from the NCBI Taxonomy as well. The main ontology can be browsed in OntoBee. All purls resolve to OntoBee.
Proper citation: eagle-i research resource ontology (RRID:SCR_008784) Copy
http://purl.bioontology.org/ontology/ADO
An open, public ontology representing relevant knowledge on Alzheimer's disease.
Proper citation: Alzheimer's disease ontology (RRID:SCR_010289) Copy
http://purl.bioontology.org/ontology/FAO
A structured controlled vocabulary for the anatomy of fungi.
Proper citation: Fungal Gross Anatomy Ontology (RRID:SCR_010322) Copy
http://purl.bioontology.org/ontology/EHDAA
A structured controlled vocabulary of stage-specific anatomical structures of the human. It has been designed to mesh with the mouse anatomy and incorporates each Carnegie stage of development (CS1-20). The abstract version of the human developmental anatomy ontology compresses all the tissues present over Carnegie stages 1-20 into a single hierarchy. The heart, for example, is present from Carnegie Stage 9 onwards and is thus represented by 12 EHDA IDs (one for each stage). In the abstract mouse, it has a single ID so that the abstract term given as just ''heart'' really means ''heart (CS 9-20)''. Timing details will be added to the abstract version of the ontology in a future release.
Proper citation: Human Developmental Anatomy Ontology abstract version 1 (RRID:SCR_010323) Copy
http://purl.bioontology.org/ontology/BAO-GPCR
Ontology (http://www.bioassayontology.org/bao_gpcr) that describes pharmacology, biochemistry and physiology of these important and therapeutically promising class of academic and pharmaceutical research targets. Incorporation and comparison of various small molecule screening data sets, such as those deposited in PubChem, ChEMBL, KEGG, PDSP, and/or IUPHAR databases, requires a formalized electronic organization system. In order to bridge the gap between the overflow of HTS data and the bottleneck of integrated analysis tools, herein, we provide the first comprehensive GPCR ontology. The development and utility of GPCR ontology was based on previously developed BioAssay Ontology (BAO). The GPCR ontology contains information about biochemical, pharmacological, and functional properties of individual GPCRs as well as GPCR-selective ligands inclusive of their HTS screening results and other records. This provides the first all-inclusive GPCR ontology with all available data to model the relationship between the GPCR binding sites and their physiologic and pharmacologic role in physiology via small molecule chemical structures. We developed this system using emerging semantic technologies, by leveraging existing and descriptive domain level ontologies.
Proper citation: G Protein-Coupled Receptor BioAssays Ontology (RRID:SCR_010324) Copy
http://purl.bioontology.org/ontology/GALEN
A translation of the full Galen ontology (from the OpenGALEN project) into the OWL description logic.
Proper citation: Galen Ontology (RRID:SCR_010325) Copy
http://purl.bioontology.org/ontology/GO-EXT
An extension of the Gene Ontology.
Proper citation: Gene Ontology Extension (RRID:SCR_010327) Copy
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