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Q28588664-14024A84-FBB8-4EE4-833F-CF11370A761A
Q28588664-14024A84-FBB8-4EE4-833F-CF11370A761A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-14024A84-FBB8-4EE4-833F-CF11370A761A
NIPA1(SPG6), the basis for autosomal dominant form of hereditary spastic paraplegia, encodes a functional Mg2+ transporter
P2860
Q28588664-14024A84-FBB8-4EE4-833F-CF11370A761A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28588664-14024A84-FBB8-4EE4-833F-CF11370A761A
rank
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type
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Statement
wasDerivedFrom
04bac335be7845d5b5ed1fa7156111bf2280396f
P2860
Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons