About: NOTCH3 gene

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An Entity of Type : about:gngm#this, within Data Space : semmed.demo.openlinksw.com associated with source document(s)

Attributes	Values
type	gngm
label	NOTCH3 gene notch3 gene
http://semmed.demo...com/terms#part_of	Zebrafish
http://semmed.demo...s#associated_with	Pathogenesis Ovarian Carcinoma
http://semmed.demo...terms#location_of	Mutation
http://semmed.demo...ms#interacts_with	Cells
http://semmed.demo...com/terms#affects	Malignant Neoplasms
http://semmed.demo...om/terms#inhibits	MBP gene\|MBP
terms:part_of	C0030705 Family Human Mus Extracellular Zebrafish Monozygotic twins 19p13 19p13.1
terms:causes	Disease Degenerative abnormality Infarction Leukoencephalopathy Disorder of artery CADASIL
terms:location_of	Mutation Polymorphism, Genetic Mutation, Missense
terms:interacts_with	Cells cerebrolysin
terms:affects	Malignant Neoplasms Amino Acid Substitution
terms:coexists_with	Promoter Regions (Genetics)
terms:compared_with	NOTCH1 gene
terms:inhibits	gamma-secretase MBP gene\|MBP Eosinophilic major basic protein\|MBP
terms:associated_with	Disease Pathogenesis Infarction Migraine Disorders Ovarian Carcinoma Cerebral Infarction Leukoencephalopathy Disorder of artery CADASIL
terms:neg_associated_with	Multiple Sclerosis
terms:predisposes	Hypertrophy Migraine Disorders
terms:higher_than	NOTCH1 gene
terms:augments	Encounter due to genetic counseling
terms:neg_part_of	Mus
terms:neg_predisposes	Cerebrovascular Disorders
LOCATION_OF	Mutation
ASSOCIATED_WITH	Ovarian Carcinoma CADASIL
schema:identifier	C1417768 c1417768
CAUSES	CADASIL
AFFECTS	Amino Acid Substitution
PREDISPOSES	Migraine Disorders
is http://semmed.demo.../terms#process_of of	Mutation Mutation, Missense
is http://semmed.demo...s#associated_with of	Infarction
is http://semmed.demo...terms#location_of of	C0030705 Family Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 19
is terms:process_of of	Mutation Mutate Polymorphism, Genetic Mutation, Missense Splice-Site Mutation Point Mutation
is terms:part_of of	Cysteine Exons
is terms:location_of of	C0030705 Family Arteries Population Group Mus Leukocytes Tail cohort Elderly father Structure of arteriole Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 19
is terms:interacts_with of	Single Nucleotide Polymorphism
is terms:affects of	Mutation pleiotropism
is terms:uses of	Molecular Diagnosis
is terms:coexists_with of	Single Nucleotide Polymorphism DNA Exons Introns
is terms:associated_with of	Infarction
is terms:neg_process_of of	Mutation
is LOCATION_OF of	C0030705

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