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Namespace Prefixes

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n3	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
dc	http://purl.org/dc/elements/1.1/
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

_:vb50946095

rdf:type

owl:Axiom

wdrs:describedby

n6:doid.owl

dc:type

n3:ECO_0007636 n3:ECO_0007645

owl:annotatedProperty

n3:IAO_0000115

owl:annotatedSource

n3:DOID_0112107

owl:annotatedTarget

A neuroacanthocytosis characterized by absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, compensated hemolysis, and involuntary movements that has_material_basis_in mutation in XK on chromosome Xp21.1.

obo:hasDbXref

url:https://medlineplus.gov/genetics/condition/mcleod-neuroacanthocytosis-syndrome/ url:https://pubmed.ncbi.nlm.nih.gov/17683354/ url:https://pubmed.ncbi.nlm.nih.gov/8004674/