Personal tools

Difference between revisions of "DOID:0080014"

From FANTOM5_SSTAR

Jump to: navigation, search
(Created page with "{{DOID |id=DOID:0080014 |name=chromosomal disease |namespace= |def= |xref= |is_a=DOID:0050177 |synonym= |comment= |alt_id= |disjoint_from= |union_of= |created_by= ...")
 
Line 2: Line 2:
 
|id=DOID:0080014
 
|id=DOID:0080014
 
|name=chromosomal disease
 
|name=chromosomal disease
|namespace=
+
|namespace=disease_ontology
 
|def=
 
|def=
 
|xref=
 
|xref=
Line 20: Line 20:
 
|located_in=
 
|located_in=
 
|part_of=
 
|part_of=
 +
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo
 +
|is_obsolete=
 +
|preceded_by=
 
}}
 
}}

Revision as of 04:59, 11 June 2012

Name:chromosomal disease
Namespace:disease_ontology

Ontology association
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.

link to ontology dataset
data


Parents

is_a:DOID:0050177(monogenic disease)



Children


is a:DOID:11983 (Prader-Willi syndrome),DOID:14250 (Down syndrome),DOID:14447 (gonadal dysgenesis)

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Human (Homo sapiens)

... further results Mouse (Mus musculus)

... further results

Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:0080014 (chromosomal disease), sorted by p-values
Analyst: Hideya Kawaji

link to source dataset
human : data
mouse : data


No analysis results