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DOID:450: Difference between revisions

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|located_in=
|located_in=
|name=myotonic disease
|name=myotonic disease
|namespace=disease_ontology
|namespace=FANTOM
|obo_creation_date=
|obo_creation_date=
|part_of=
|part_of=

Latest revision as of 16:51, 12 September 2014

Name:myotonic disease
Namespace:FANTOM
Xrefs:
links:

ICD9CM:359.2
MSH:D020967
NCI:C84913
SNOMEDCT_2010_1_31:155096007
SNOMEDCT_2010_1_31:193237003
SNOMEDCT_2010_1_31:193240003
SNOMEDCT_2010_1_31:267713009

UMLS_CUI:C0553604

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:423(myopathy)



Children


is a:DOID:11722 (myotonic dystrophy)

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:450 (myotonic disease), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data