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bn:00193010n
Noun Named Entity
SYL
No term available
EN
SLC22A5 is a membrane transport protein associated with primary carnitine deficiency. Wikipedia
English:
gene
Relations
Sources
IS A
EN
gene
CHROMOSOME
EN
chromosome 5
FOUND IN TAXON
homo sapiens
GENETIC ASSOCIATION
EN
asthma
EN
systemic primary carnitine deficiency

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