Ontology for MicroRNA Target

Last uploaded: January 5, 2021

Preferred Name	Hereditary Central Nervous System Demyelinating Diseases
Synonyms
ID	http://purl.obolibrary.org/obo/OMIT_0020188
label	Hereditary Central Nervous System Demyelinating Diseases
prefixIRI	OMIT:0020188
prefLabel	Hereditary Central Nervous System Demyelinating Diseases
subClassOf	http://purl.obolibrary.org/obo/OMIT_0020181 http://purl.obolibrary.org/obo/OMIT_0004990 http://purl.obolibrary.org/obo/OMIT_0020587 http://purl.obolibrary.org/obo/OMIT_0026728

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Mapping To	Ontology	Source
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.132.100.362	RH-MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D020279	RH-MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.648.189.362	RH-MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.574.500.494	RH-MESH	LOOM
http://bioontology.org/projects/ontologies/birnlex#birnlex_12526	BIRNLEX	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.163.100.362	RH-MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.400.367	RH-MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.314.400	RH-MESH	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.565.189.362	RH-MESH	LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038277	PMAPP-PMO	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.695.625	RH-MESH	LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12526	NIFDYS	LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12526	NIFSTD	LOOM
http://id.nlm.nih.gov/mesh/D020279	MDM	LOOM
http://purl.bioontology.org/ontology/MESH/D020279	MESH	LOOM
http://purl.jp/bio/4/id/200906069317139540	IOBC	LOOM