DOID:936: Difference between revisions
From FANTOM5_SSTAR
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|id=DOID:936
|name=brain disease
|namespace=
|def=
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|is_a=DOID:331
|synonym="encephalopathy" EXACT []
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|alt_id=DOID:8510
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|id=DOID:936 | |id=DOID:936 | ||
|name=brain disease | |name=brain disease | ||
|namespace= | |namespace=disease_ontology | ||
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|xref= | |xref=MSH:D001927;;SNOMEDCT_2010_1_31:155053002;;SNOMEDCT_2010_1_31:193051008;;SNOMEDCT_2010_1_31:76011009;;SNOMEDCT_2010_1_31:81308009;;UMLS_CUI:C0006111;;UMLS_CUI:C0085584 | ||
|is_a=DOID:331 | |is_a=DOID:331 | ||
|synonym="encephalopathy" EXACT [] | |synonym="encephalopathy" EXACT [] | ||
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|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo | |||
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Revision as of 14:01, 11 June 2012
| Name: | brain disease | ||
|---|---|---|---|
| Namespace: | disease_ontology | ||
| Xrefs: |
| ||
| Synonyms: | "encephalopathy" EXACT [] | ||
| Alt_id: | DOID:8510 |
Ontology association<br>Each term has an is_a parent in the Disease Ontology, which has a linkage to an another entity and FANTOM5 samples.Libraries were grouped into mutually exclusive facets according to the FANTOM5 sample ontology mapping to DISEASE ontologies.<br><br>link to ontology dataset<br>data
Parents
| is_a: | DOID:331(central nervous system disease) |
|---|
Children
| is a: | DOID:1443 (cerebral degeneration) |
|---|
Ontology Tree: Loaded from BioPortal
Ontorolgy tree(Small window open)
FF samples
Human (Homo sapiens)
Mouse (Mus musculus)
Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:936 (brain disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
No analysis results
