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<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: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 <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data


No analysis results