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Difference between revisions of "DOID:0080014"

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{{DOID
 
{{DOID
|id=DOID:0080014
+
|alt_id=
|name=chromosomal disease
 
|namespace=disease_ontology
 
|def=
 
|xref=
 
|is_a=DOID:0050177
 
|synonym=
 
 
|comment=
 
|comment=
|alt_id=
 
|disjoint_from=
 
|union_of=
 
 
|created_by=
 
|created_by=
|obo_creation_date=
+
|def=
|subset=
 
 
|derives_from=
 
|derives_from=
 
|develops_from=
 
|develops_from=
 +
|disjoint_from=
 
|has_quality=
 
|has_quality=
 +
|id=DOID:0080014
 +
|is_a=DOID:630
 +
|is_obsolete=
 
|located_in=
 
|located_in=
 +
|name=chromosomal disease
 +
|namespace=disease_ontology
 +
|obo_creation_date=
 
|part_of=
 
|part_of=
 +
|preceded_by=
 
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo
 
|property_value=IAO:0000412 file:/Users/cjm/Dropbox/fantom5/HumanDO.obo
|is_obsolete=
+
|subset=
|preceded_by=
+
|synonym=
 +
|union_of=
 +
|xref=
 
}}
 
}}

Revision as of 01:32, 12 September 2014

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:630(genetic 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