DOID:2355
From FANTOM5_SSTAR
Name: | anemia | ||
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Namespace: | FANTOM | ||
Xrefs: |
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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:74(hematopoietic system disease) |
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Children
is a: | FF:10808-111A7 (hereditary spherocytic anemia cell line:WIL2-NS) |
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Ontology Tree: Loaded from BioPortal
Ontorolgy tree(Small window open)
FF samples
Human (Homo sapiens)
- 10808-111A7 (hereditary spherocytic anemia cell line:WIL2-NS)
Mouse (Mus musculus)
- 10808-111A7 (hereditary spherocytic anemia cell line:WIL2-NS)
Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:2355 (anemia), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data
P-value | FFCP | Short description |
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