DOID:0080014: Difference between revisions
From FANTOM5_SSTAR
(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=
...") |
No edit summary |
||
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 13:59, 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)
- 10521-107E8
- 10804-111A3
- 10806-111A5
- 10814-111B4
- 13445-144F7 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
- 13446-144F8 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
- 13447-144F9 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
- 13448-144G1 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
- 13449-144G2 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
- 13450-144G3 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
... further results Mouse (Mus musculus)
- 10521-107E8
- 10804-111A3
- 10806-111A5
- 10814-111B4
- 13445-144F7 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
- 13446-144F8 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
- 13447-144F9 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
- 13448-144G1 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
- 13449-144G2 (iPS differentiation to neuron, down-syndrome donor C11-CCL54)
- 13450-144G3 (iPS differentiation to neuron, down-syndrome donor C18-CCL54)
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