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asEquivalent
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b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
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About:
chromosome 1q deletion syndrome
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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
type
dsyn
label
chromosome 1q deletion syndrome
terms:process_of
Individual
terms:coexists_with
Microcephaly
schema:identifier
C0795799
c0795799
PROCESS_OF
Individual
is
terms:location_of
of
1q32.1
is
terms:coexists_with
of
Hydrocephalus
Congenital absence
is
terms:associated_with
of
mismatch repair protein 1|MSH3|CDT1
CDT1 Gene|MSH3|CDT1
is
terms:neg_coexists_with
of
Hypogammaglobulinemia
Congenital Hydrocephalus
is
LOCATION_OF
of
1q32.1
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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