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http://www.w3.org/2002/07/owl#
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About:
7p13
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An Entity of Type :
about:nusq#this
, within Data Space :
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associated with source
document(s)
Type:
nusq
New Facet based on Instances of this Class
Attributes
Values
type
nusq
label
7p13
terms:part_of
Chromosomes, Human
terms:location_of
Syndrome
Malignant neoplasm of brain
Craniosynostosis
Greig cephalopolysyndactyly syndrome
terms:affects
Lymphocyte
terms:coexists_with
Single Nucleotide Polymorphism
RUNX2
GLI3 gene|GLI3
EDAR
9q22
DCHS2
GLI3 gene|GLI3
terms:associated_with
Dysmyelopoietic Syndromes
DELETION
Structural Chromosomal Abnormality
Greig cephalopolysyndactyly syndrome
LOCATION_OF
Greig cephalopolysyndactyly syndrome
schema:identifier
C1521616
c1521616
PART_OF
Chromosomes, Human
is
terms:part_of
of
EGF
GLI3 gene|GLI3
TRBV20OR9-2
c-erbB-1 Proto-Oncogenes|EGFR
Genes, Developmental
Phosphoglycerate Mutase
GLI3 gene|GLI3
URGCP
is
terms:location_of
of
C0030705
Chromosomes, Human, Pair 7
is
terms:coexists_with
of
Genes
GLI3 gene|GLI3
GLI3 gene|GLI3
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