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Q36770065-1C94F359-C0D8-496F-9E4C-E0EC094D7A96
Q36770065-1C94F359-C0D8-496F-9E4C-E0EC094D7A96
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36770065-1C94F359-C0D8-496F-9E4C-E0EC094D7A96
Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population
P2860
Q36770065-1C94F359-C0D8-496F-9E4C-E0EC094D7A96
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36770065-1C94F359-C0D8-496F-9E4C-E0EC094D7A96
rank
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type
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Statement
wasDerivedFrom
e5532254ea4a783d957e064e1e971e5f2c835588
P2860
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter