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About:
primary ovarian insufficiency 2B
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
X-linked recessive disease
primary ovarian insufficiency
nodeID://b50941761
label
primary ovarian insufficiency 2B
(en)
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0080859
database_cross_reference
OMIM:300604
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A primary ovarian insufficiency that has_material_basis_in mutation in the POF1B gene.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50941762
Faceted Search & Find service v1.17_git149 as of Dec 03 2024
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