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Rule:
asEquivalent
b3s
b3sifp
facets
http://www.w3.org/2002/07/owl#
ldp
oplweb
skos-trans
virtrdf-eturtle-containers
virtrdf-hashtag
virtrdf-ifp
virtrdf-label
virtrdf-meta-entity-class
None
Inverse Functional Properties:
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Apply to subjects only
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About:
PAX6
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An Entity of Type :
semmed:Gene
, within Data Space :
semmed.demo.openlinksw.com
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
label
pax6
NEG_PART_OF
Mus
Lens, Crystalline
ES Cell Line
LOCATION_OF
Mutation
Transcriptional Activation
DNA Binding
Protein Expression
Loss of Heterozygosity
Ectopic Expression
COEXISTS_WITH
Amino Acids
Insulin|INS
Genes, Homeobox
CRYGD
Alar
NANOG
MLL2 gene|KMT2D|KMT2B
BMP4|BMP4
ENG gene|ENG
MLL gene|KMT2A
SETD1A
MEIS2
NEG_AFFECTS
DNA Binding
Cell Proliferation
ASSOCIATED_WITH
Disease
Pathogenesis
Diabetes Mellitus
Pancreatic carcinoma
Degenerative abnormality
Primary Neoplasm
Adenocarcinoma pancreas
Alcoholic Intoxication, Chronic
Glioblastoma
Sleeplessness
Myopia
Keratitis
Ocular surface disease
Idiopathic generalized epilepsy
Squamous metaplasia
schema:identifier
5080
INHIBITS
Genes
Bone Morphogenetic Proteins
Transforming Growth Factor beta
Fatty Acid-Binding Proteins
Neuropilin-1|NRP1
NES gene|NES
SHH gene|SHH
NRP2
PAX3 gene|PAX3
delta-catenin
PAX2
EN1
CDCA7
TECTA gene|TECTA
PART_OF
Mammals
Cells
Cytoplasm
Cell Nucleus
C0030705
Family
Eye
Retina
Human
member
Child
Fetus
granule cell
Mus
House mice
Zebrafish
Canis familiaris
Inner Nuclear Layer
Goldfish
Ganglion Cell Layer
Optic vesicle
Dicyema
CAUSES
Disease
Cessation of life
Mental Retardation
Congenital Abnormality
Up-Regulation (Physiology)
Neural Development
OCULAR DEFECT
Keratitis
Autistic Disorder
Eye diseases
Eye Abnormalities
Aniridia
Microcornea
Microphthalmos
Infantile nystagmus syndrome
INTERACTS_WITH
Genes
Cells
DNA
Neurons
Cell Line
Gelatinase A
Tretinoin
genetic element
Neuroglia
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