About: ATP1A3 gene|ATP1A3

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An Entity of Type : http://semmed.demo.openlinksw.com/schemas/Gene#this, within Data Space : semmed.demo.openlinksw.com associated with source document(s)

Attributes	Values
type	ATP1A3 gene\|ATP1A3 Semmed Gene Class
label	ATP1A3 gene\|ATP1A3 atp1a3 gene atp1a3
sameAs	ATP1A3 (NIH - Gene) ATP1A3
http://semmed.demo...s#associated_with	Parkinsonian Disorders
http://semmed.demo....com/terms#causes	Hemiplegia, Crossed
http://semmed.demo...ms#interacts_with	Neurons Myocytes, Cardiac
terms:part_of	Child
terms:causes	nervous system disorder Parkinsonian Disorders Hemiplegia, Crossed
terms:location_of	Mutation Mutation, Missense Point Mutation
terms:interacts_with	Neurons Myocytes, Cardiac
terms:coexists_with	SLC2A1 gene\|SLC2A1
terms:associated_with	Epilepsy Parkinsonian Disorders
LOCATION_OF	Mutation
ASSOCIATED_WITH	Epilepsy Parkinsonian Disorders
schema:identifier	478 C1412630\|478 c1412630
PART_OF	Child
CAUSES	nervous system disorder
is type of	ATP1A3 gene\|ATP1A3
is http://semmed.demo.../terms#process_of of	Mutation
is http://semmed.demo...terms#location_of of	Chromosomes, Human, Pair 2
is terms:process_of of	Mutation Mutation, Missense
is terms:location_of of	C0030705 Neurons Child Chromosomes, Human, Pair 2
is terms:affects of	Mutation
is terms:neg_process_of of	Mutation
is PROCESS_OF of	Mutation

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