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 _:vb50941610
rdf:type
owl:Axiom
wdrs:describedby
n5:doid.owl
owl:annotatedProperty
n6:IAO_0000115
owl:annotatedSource
n6:DOID_0080773
owl:annotatedTarget
A beta thalassemia that is characterized by decreased or absent synthesis of both the delta- and beta-globin chains, which leads to a compensatory increase in fetal gamma-chain synthesis. This disorder results in a microcytic anemia that is clinically mild.
obo:hasDbXref
url:https://pubmed.ncbi.nlm.nih.gov/30706898/
url:https://pubmed.ncbi.nlm.nih.gov/31444804/