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{{DOID
{{DOID
|id=DOID:3149
|alt_id=
|name=keratoacanthoma
|namespace=disease_ontology
|def=
|xref=MSH:D007636;;NCI:C3146;;SNOMEDCT_2010_1_31:156395005;;SNOMEDCT_2010_1_31:201061007;;SNOMEDCT_2010_1_31:201064004;;SNOMEDCT_2010_1_31:254662007;;SNOMEDCT_2010_1_31:267858008;;SNOMEDCT_2010_1_31:58220003;;UMLS_CUI:C0022572
|is_a=DOID:3151
|synonym="keratoacanthoma" EXACT [CSP2005:2020-2121];;"keratoacanthoma" EXACT [MTH:NOCODE];;"Keratoacanthoma (disorder)" EXACT [SNOMEDCT_2005_07_31:254662007];;"Keratoacanthoma (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:58220003]
|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:3149
|is_a=DOID:3151
|is_obsolete=
|located_in=
|located_in=
|name=keratoacanthoma
|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="keratoacanthoma" EXACT [CSP2005:2020-2121];;"keratoacanthoma" EXACT [MTH:NOCODE];;"Keratoacanthoma (disorder)" EXACT [SNOMEDCT_2005_07_31:254662007];;"Keratoacanthoma (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:58220003]
|union_of=
|xref=MSH:D007636;;NCI:C3146;;SNOMEDCT_2010_1_31:156395005;;SNOMEDCT_2010_1_31:201061007;;SNOMEDCT_2010_1_31:201064004;;SNOMEDCT_2010_1_31:254662007;;SNOMEDCT_2010_1_31:267858008;;SNOMEDCT_2010_1_31:58220003;;UMLS_CUI:C0022572
}}
}}

Revision as of 10:34, 12 September 2014

Name:keratoacanthoma
Namespace:disease_ontology
Xrefs:
links:

MSH:D007636
NCI:C3146
SNOMEDCT_2010_1_31:156395005
SNOMEDCT_2010_1_31:201061007
SNOMEDCT_2010_1_31:201064004
SNOMEDCT_2010_1_31:254662007
SNOMEDCT_2010_1_31:267858008
SNOMEDCT_2010_1_31:58220003

UMLS_CUI:C0022572
Synonyms: "keratoacanthoma" EXACT [CSP2005:2020-2121]
"keratoacanthoma" EXACT [MTH:NOCODE]
"Keratoacanthoma (disorder)" EXACT [SNOMEDCT_2005_07_31:254662007]
"Keratoacanthoma (morphologic abnormality)" EXACT [SNOMEDCT_2005_07_31:58220003]

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:3151(skin squamous cell carcinoma)



Children


is a:FF:10713-109I2 (),FF:10791-110H8 (keratoacanthoma cell line:HKA-1)

Ontology Tree: Loaded from BioPortal

Ontorolgy tree(Small window open)

FF samples

Human (Homo sapiens)

Mouse (Mus musculus)

Enrichment analysis: top 100 FFCP enriched with this ontology termTOP 100 FANTOM5 Cage Peaks enriched with DOID:3149 (keratoacanthoma), sorted by p-values <br>Analyst: Hideya Kawaji<br><br>link to source dataset <br>human : data <br>mouse : data