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Neuroscience Information Framework (NIF) Standard Ontology
Acronym | NIFSTD |
Visibility | Public |
Description | NIF Standard ontology (NIFSTD) is a core component of Neuroscience Information Framework (NIF) project (http://neuinfo.org), a semantically enhanced portal for accessing and integrating neuroscience data, tools and information. NIFSTD includes a set of modular ontologies that provide a comprehensive collection of terminologies to describe neuroscience data and resources. |
Status | Production |
Format | OWL |
Contact | Tom Gillespie, tgbugs@gmail.com |
Categories | All Organisms, Anatomy, Biological Process, Cell, Cellular anatomy , Dysfunction, Molecule, Neurologic Disease, Neurological Disorder, Other, Subcellular, Subcellular anatomy |
Version | Released | Uploaded | Downloads |
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3.1 - January 15, 2018 (Parsed, Indexed, Metrics, Annotator) | 02/10/2018 | 02/10/2018 | OWL | CSV | RDF/XML | Diff |
3.1 - January 15, 2018 (Archived) | 02/05/2018 | 02/05/2018 | OWL | Diff |
3.1 - January 15, 2018 (Archived) | 01/15/2018 | 01/15/2018 | OWL | Diff |
3.0 - October 16, 2017 (Archived) | 12/03/2017 | 12/03/2017 | OWL | Diff |
3.0 - October 16, 2017 (Archived) | 10/16/2017 | 10/16/2017 | OWL | Diff |
2.12 - July 7, 2016 (Archived) | 10/10/2017 | 10/10/2017 | OWL | Diff |
2.10 - February 10, 2015 (Archived) | 02/13/2016 | 02/13/2016 | OWL | Diff |
2.10 - February 10, 2015 (Archived) | 10/09/2015 | 10/09/2015 | OWL | Diff |
2.10 - February 10, 2015 (Archived) | 10/08/2015 | 10/08/2015 | OWL | Diff |
2.10 - February 10, 2015 (Archived) | 02/13/2015 | 02/13/2015 | OWL | Diff |
2.9.6.1 - September 3, 2013 (Archived) | 09/03/2013 | 09/03/2013 | OWL | Diff |
2.9.6 - July 18, 2013 (Archived) | 08/05/2013 | 08/05/2013 | OWL | Diff |
2.9.1 - January 23, 2012 (Archived) | 01/23/2013 | 01/30/2013 | OWL | Diff |
2.8.2 - June 21, 2012 (Archived) | 06/22/2012 | 06/22/2012 | OWL | Diff |
2.8.1 - May 25, 2012 (Archived) | 06/06/2012 | 06/06/2012 | OWL |
2.5 - October 17, 2011 (Archived) | 10/17/2011 | 11/18/2011 | OWL |
2.3 - June 10, 2011 (Archived) | 06/14/2011 | 06/14/2011 | OWL |
2.2 - December 20, 2010 (Archived) | 03/08/2011 | 03/08/2011 | OWL |
1.9.5 (Archived) | 08/13/2010 | 08/13/2010 | OWL |
1.8 (Archived) | 03/30/2010 | 04/12/2010 | OWL |
1.4 (Archived) | 10/14/2009 | 10/23/2009 | OWL |
1.3 (Archived) | 07/05/2009 | 08/18/2009 | OWL |
1 (Archived) | 03/10/2009 | 08/17/2009 | OWL |
0.5 (Archived) | 09/04/2007 | 02/26/2008 | OWL |
more... |
- NIF - Resource Type Hieracrchy (view)
- This is a view of NIFSTD (version 2.82) containing the Resource Type Hierarchy.
Classes | 177,974 |
Individuals | 477 |
Properties | 894 |
Maximum depth | 0 |
Maximum number of children | 17,188 |
Average number of children | 5 |
Classes with a single child | 21,719 |
Classes with more than 25 children | 749 |
Classes with no definition | 66,593 |
Id | http://uri.neuinfo.org/nif/nifstd/birnlex_12565
http://uri.neuinfo.org/nif/nifstd/birnlex_12565
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Preferred Name | Motor Neuron Disease |
Definitions |
Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy ( BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation (MeSH).
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Synonyms |
Motor System Disease
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
definition | Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy ( BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation (MeSH). |
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alternative label | Motor System Disease
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preferred label | Motor Neuron Disease
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label | Motor Neuron Disease
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externalSourceId |
C0085084
D016472
_8.3_2.5
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UmlsCui | C0085084
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synonym | Motor System Disease
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hasExternalSource | |
createdDate | October 5, 2007
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note | Diseases characterized by a selective degeneration of the motor neurons of the spinal cord, brainstem, or motor cortex. Clinical subtypes are distinguished by the major site of degeneration. In AMYOTROPHIC LATERAL SCLEROSIS there is involvement of upper, lower, and brainstem motor neurons. In progressive muscular atrophy and related syndromes (see MUSCULAR ATROPHY, SPINAL) the motor neurons in the spinal cord are primarily affected. With progressive bulbar palsy ( BULBAR PALSY, PROGRESSIVE), the initial degeneration occurs in the brainstem. In primary lateral sclerosis, the cortical neurons are affected in isolation (MeSH).
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usageNote | Note that MeSH includes the following sub-types which cannot easily be specified as subtypes without leading to multiple inheritance (e.g., Anterior Horn Cell Disease; Familial Motor Neuron Disease; Lateral Sclerosis; Lower Motor Neuron Disease; Upper Motor Neuron Disease; Primary Lateral Sclerosis; Secondary Motor Neuron Disease). These subtypes describe either the location within the CNS axis where motor neuron degeneration is observed, the complex temporal development of that degeneration, and the hereditory nature of the disorder. In the course of many specific patient cases, the location of degenerating MNs starts in one location and then procedes to others, as is the case for some of the concrete child classess created for this parent class. In the end, a more detailed OWL representation would need to be employed where the location, timing, and putative casue of degenerating MNs is specified using ObjectProperties, and such subtypes as LOWER MOTOR NEURON DISEASE would then be inferred types. The practical problem with this approach is that terms such as ALS and LOWER MN DISEASE have a particular meaning in a clinical context. Though ALS might be inferred to be a member of the set of LOWER MN DISEASEs, since there is loss of MNs in the lower spinal cord, clinicians typically consider LOWER MN DISEASE to have a distinct set of presenting signs when compared to ALS. Clinicians do not typically consider ALS to be a type of LOWER MN DISEASE (BB: 2007-10-05)
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definingCitationURI | |
hasCurationStatus | |
MeshUid | D016472
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subClassOf | |
hasDefinitionSource | |
Resource Identifier |
C0085084
D016472
_8.3_2.5
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hasBirnlexCurator | |
editorial note | |
type | |
modifiedDate | November 18, 2007
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nifID | _8.3_2.5
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definingCitation | Adams et al., Principles of Neurology, 6th ed, p1089
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Delete | Subject | Author | Type | Created |
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No notes to display |
- Problem retrieving properties:
Notes
Subject | Author | Type | Class | Created |
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Replacement term needed | whetzel | Comment | http://ontology.neuinfo.org/NIF/Backend/BIRNLex-OBI-proxy.owl#birnlex_11002 | 2009-11-15 |
IAO equivalent term | whetzel | Comment | http://ontology.neuinfo.org/NIF/Backend/BIRNLex-OBI-proxy.owl#birnlex_11037 | 2009-11-15 |
Add NCBO Web Widgets to your site for NIFSTD
Widget type | Widget demonstration |
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Step 2: Follow the Instructions
For more help visit NCBO Widget Wiki |
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Example 1 (start typing the class name to get its full URI)
Example 2 (get the ID for a class) Example 3 (get the preferred name for a class) Step 2: Follow the Instructions
For more help visit NCBO Widget Wiki |
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Step 2: Follow the InstructionsCopy the code below and paste it to your HTML page <iframe frameborder="0" src="/widgets/visualization?ontology=NIFSTD&class=http%3A%2F%2Fpurl.obolibrary.org%2Fobo%2FGO_1903994&apikey=YOUR_API_KEY"></iframe> For more help visit NCBO Widget Wiki |
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Step 2: Follow the InstructionsCopy the code below and paste it to your HTML page <link rel="stylesheet" type="text/css" href="/widgets/jquery.ncbo.tree.css"> <script src="/widgets/jquery.ncbo.tree-2.0.2.js"></script> <div id="widget_tree"></div> var widget_tree = $("#widget_tree").NCBOTree({ apikey: "YOUR_API_KEY", ontology: "NIFSTD" }); You can also view a detailed demonstration For more help visit NCBO Widget Wiki |