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Q28588664-1EC47494-BF63-45AA-95A5-A47100D209FB
Q28588664-1EC47494-BF63-45AA-95A5-A47100D209FB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-1EC47494-BF63-45AA-95A5-A47100D209FB
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
P921
Q28588664-1EC47494-BF63-45AA-95A5-A47100D209FB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-1EC47494-BF63-45AA-95A5-A47100D209FB
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
17da9be1f8890cd10616e848aec6b571eb80d078
P921
Non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)