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asEquivalent
b3s
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facets
http://www.w3.org/2002/07/owl#
ldp
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About:
Lipid storage myopathy
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An Entity of Type :
about:dsyn#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
Type:
dsyn
New Facet based on Instances of this Class
Attributes
Values
label
lipid storage myopathy
COEXISTS_WITH
Infantile disease
Deficiency of butyryl-CoA dehydrogenase
Glycogen Storage Disease Type I
Familial hyperlipoproteinemia
schema:identifier
c0410214
PROCESS_OF
C0030705
Human
Canis familiaris
sibling
Older sibling
Spaniel
is
COEXISTS_WITH
of
Contracture
Obstruction
Scoliosis, unspecified
Carnitine deficiency
is
ASSOCIATED_WITH
of
Creatine Kinase
is
DIAGNOSES
of
Muscle biopsy
Magnetic Resonance Imaging
is
CAUSES
of
Mutation
Carnitine deficiency
is
TREATS
of
Diagnosis
Levocarnitine
Carnitine
Medium chain triglycerides
Therapeutic diets
is
AFFECTS
of
Disease
Malignant hyperpyrexia due to anesthesia
Riboflavin
genetic analysis
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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