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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/VHOG
A multi-species anatomical ontology for the vertebrate lineage, developed as part of the Bgee project. The mapping to species-specific anatomical ontologies is provided as a separated file: http://bgee.unil.ch/download/organ_association_vHOG.txt This mapping represents homology-strict relationships, in the sense of HOM:0000007 historical homology. Each mapping has been manually reviewed, and theye provide confidence codes and references when available.
Proper citation: Vertebrate Homologous Organ Group Ontology (RRID:SCR_010444) 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/VANDF, NDF
Ontology that includes information on clinical drugs, drug classes, ingredients and National Drug Code (NDC) Directory codes.
Proper citation: Veterans Health Administration National Drug File (RRID:SCR_010445) 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/VSO
An extension of the Ontology for General Medical Science (OGMS) that covers the four consensus human vital signs: blood pressure, body temperature, respiration rate, pulse rate. VSO provides also a controlled structured vocabulary for describing vital signs measurement data, the various processes of measuring vital signs, and the various devices and anatomical entities participating in such measurements.
Proper citation: Vital Sign Ontology (RRID:SCR_010446) Copy
http://purl.bioontology.org/ontology/GO-EXT
An extension of the Gene Ontology.
Proper citation: Gene Ontology Extension (RRID:SCR_010327) Copy
http://purl.bioontology.org/ontology/GENE-CDS
Ontology to unify several functionalities in a single resource, being: * A knowledge base for clinical pharmacogenomics/pharmacogenetics that can be used for question-answering (e.g., which SNPs are associated with this drug?) * A rule base for clinical decision support (e.g., inferring that a patient with a specific set of SNPs requires a lowered dose of warfarin and generating a CDS message that can be viewed by clinicians) * A tool for checking data consistency (e.g., highlighting which allele definitions in PharmGKB are overlapping, or which clinical decision support rules are matching the same group of patients)
Proper citation: Genomic Clinical Decision Support Ontology (RRID:SCR_010331) Copy
http://purl.bioontology.org/ontology/GEOSPECIES
Ontology to help integrate species concepts with species occurrences, gene sequences, images, references and geographical information. See also Taxonconcept.org
Proper citation: GeoSpecies Ontology (RRID:SCR_010332) Copy
http://purl.bioontology.org/ontology/HLTHINDCTRS
Ontology for standardized health outcome and health determinant indicators as maintained by the CDC National Center for Health Statistics.
Proper citation: Health Indicator Ontology (RRID:SCR_010335) Copy
http://purl.bioontology.org/ontology/HL7
Ontology for the data types used in the creation of HL7 (Health Level Seven International) V3 specifications. This version is the first update to Normative RIM, Release 3. It is based on changes approved in Harmonization in November 2010. This release of the RIM is bound to HL7 Abstract Data Types Release 2. https://www.hl7.org/implement/standards/product_brief.cfm?product_id=264
Proper citation: Health Level Seven Reference Implementation Model Version 3 (RRID:SCR_010336) Copy
http://purl.bioontology.org/ontology/HINO
An Interaction Network Ontology (INO) extension for the domain of human interaction networks. It has currently incoporated Reactome reactions and pathways. Like INO, HINO aligns with BFO. HINO is developed by following the OBO Foundry principles.
Proper citation: Human Interaction Network Ontology (RRID:SCR_010339) Copy
http://purl.bioontology.org/ontology/IMGT-ONTOLOGY
Ontology for immunogenetics and immunoinformatics. Provides semantic specification of terms to be used in immunogenetics and immunoinformatics and manages related knowledge, thus allowing standardization for immunogenetics data from genome, proteome, genetics, two-dimensional (2D) and three-dimensional (3D) structures. Manages the knowledge through diverse facets relying on seven axioms, IDENTIFICATION, CLASSIFICATION, DESCRIPTION, NUMEROTATION, LOCALIZATION, ORIENTATION and OBTENTION. These axioms postulate that any object, any process and any relation can be identified, classified, described, numbered, localized and orientated, and the way it is obtained can be characterized. The axioms constitute the Formal IMGT-ONTOLOGY, also designated as IMGT-Kaleidoscope. As the same axioms can be used to generate concepts for multi-scale level approaches, the Formal IMGT-ONTOLOGY represents a paradigm for system biology ontologies, which need to identify, to classify, to describe, to number, to localize and to orientate objects, processes and relations at the molecule, cell, tissue, organ, organism or population levels. IMGT, the international ImMunoGeneTics information system, has been built on IMGT-ONTOLOGY. The version 1.0.2 of IMGT-ONTOLOGY includes the concepts of IDENTIFICATION and the concepts of CLASSIFICATION.
Proper citation: IMGT-ONTOLOGY (RRID:SCR_010342) Copy
http://purl.bioontology.org/ontology/IDQA
Ontology for Image and Data Quality Assessment for scientific data management.
Proper citation: Image and Data Quality Assessment Ontology (RRID:SCR_010343) Copy
http://purl.bioontology.org/ontology/SYMP
Ontology designed around the guiding concept of a symptom being: A perceived change in function, sensation or appearance reported by a patient indicative of a disease. Understanding the close relationship of Signs and Symptoms, where Signs are the objective observation of an illness, the Symptom Ontology will work to broaden it''s scope to capture and document in a more robust manor these two sets of terms. Understanding that at times, the same term may be both a Sign and a Symptom
Proper citation: Symptom Ontology (RRID:SCR_010388) Copy
http://purl.bioontology.org/ontology/STATO
A general-purpose STATistics Ontology to provide coverage for processes such as statistical tests, their conditions of applications, and information needed or resulting from statistical methods, such as probability distributions, variable, spread and variation metrics. STATO also covers aspects of experimental design and description of plots and graphical representations commonly used to provide visual cues of data distribution or layout and to assist review of the results.
Proper citation: STATistics Ontology (RRID:SCR_010421) Copy
http://purl.bioontology.org/ontology/SYN
Controlled vocabulary used for various entity properties in the Synapse platform.
Proper citation: Sage Bionetworks Synapse Ontology (RRID:SCR_010422) Copy
http://purl.bioontology.org/ontology/SEP
A structured controlled vocabulary for the annotation of sample processing and separation techniques in scientific experiments, such as, and including, gel electrophoresis, column chromatography, capillary electrophoresis, centrifugation and so on. Developed jointly by the HUPO Proteomics Standards Initiative and The Metabolomics Standards Initiative.
Proper citation: Sample Processing and Separation Techniques Ontology (RRID:SCR_010423) Copy
http://purl.bioontology.org/ontology/OBCS
A biomedical ontology in the domain of biological and clinical statistics that is primarily targeted for statistical representation in the fields in biological, biomedical, and clinical domains. It uses the Basic Formal Ontology (BFO) as the upper level ontology. OBCS imports all biostatistics related terms in the Ontology for Biomedical Investigations (OBI) including all logical axioms.
Proper citation: Ontology of Biological and Clinical Statistics (RRID:SCR_010391) Copy
http://purl.bioontology.org/ontology/OCRE
Ontology to support systematic description of, and interoperable queries on, human studies and study elements.
Proper citation: Ontology of Clinical Research (RRID:SCR_010392) Copy
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