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asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
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skos-trans
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virtrdf-ifp
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None
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About:
Muscle eye brain disease
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An Entity of Type :
about:cgab#this
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
Type:
cgab
New Facet based on Instances of this Class
Attributes
Values
label
muscle eye brain disease
schema:identifier
c0457133
ISA
Disease
PART_OF
C0030705
Child
AFFECTS
Mutation
C0030705
Point Mutation
is
LOCATION_OF
of
C0030705
Child
is
COEXISTS_WITH
of
Congenital muscular dystrophy
Congenital anomaly of brain
Eye Abnormalities
Retinal Perforations
is
DIAGNOSES
of
Magnetic Resonance Imaging
is
CAUSES
of
protein O-mannose beta-1,2-N-acetylglucosaminyltransferase|POMGNT1
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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