SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
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n6 http://purl.obolibrary.org/obo/
wdrs http://www.w3.org/2007/05/powder-s#
obo http://www.geneontology.org/formats/oboInOwl#
rdf http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl http://www.w3.org/2002/07/owl#
xsdh http://www.w3.org/2001/XMLSchema#
Statements
Subject Item _:vb50952006
rdf:type
owl:Axiom
wdrs:describedby
n4:doid.owl
owl:annotatedProperty
n6:IAO_0000115
owl:annotatedSource
n6:DOID_3491
owl:annotatedTarget
A gonadal dysgenesis that is characterized by short stature and early loss of ovarian function resulting from ovarian hypofunction or premature ovarian failure and has_material_basis_in one missing or structurally altered X chromosome.
obo:hasDbXref
url:https://rarediseases.org/rare-diseases/turner-syndrome/
url:https://ghr.nlm.nih.gov/condition/turner-syndrome