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asEquivalent
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b3sifp
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http://www.w3.org/2002/07/owl#
ldp
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About:
11p15.5
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about:nusq#this
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associated with source
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Type:
nusq
New Facet based on Instances of this Class
Attributes
Values
label
11p15.5
LOCATION_OF
Disease
Hereditary Diseases
Syndrome
Tumorigenesis
Beckwith-Wiedemann Syndrome
Bipolar Disorder
Rhabdomyosarcoma, Embryonal
Jervell-Lange Nielsen Syndrome
HEMOGLOBIN--BETA LOCUS
COEXISTS_WITH
DNA
SCTR gene|SCTR
ASSOCIATED_WITH
Malignant Neoplasms
Malignant neoplasm of breast
Neoplasm
Tumorigenesis
Beckwith-Wiedemann Syndrome
Rhabdomyosarcoma, Embryonal
Nephroblastoma
Uniparental Disomy
Chromosomal Duplication
Placental dysplasia
schema:identifier
c1520373
CAUSES
Beckwith-Wiedemann Syndrome
Chromosomal translocation
AFFECTS
Organ
Beckwith-Wiedemann Syndrome
PREDISPOSES
Neoplasms, Embryonal
is
LOCATION_OF
of
Mothers
Population Group
Koreans (ethnic group)
Rat-1
is
COEXISTS_WITH
of
DNA Sequence
SCTR gene|SCTR
Immunoglobulins
VPS51
is
PART_OF
of
Genes
H19 gene|H19|HILS1
Faceted Search & Find service v1.17_git42 as of Oct 29 2019
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