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1
Q24672217-0EAED566-EB7B-4D59-AFE6-CB9D24DA30C0
Q24672217-0EAED566-EB7B-4D59-AFE6-CB9D24DA30C0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672217-0EAED566-EB7B-4D59-AFE6-CB9D24DA30C0
Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q
P2860
Q24672217-0EAED566-EB7B-4D59-AFE6-CB9D24DA30C0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24672217-0EAED566-EB7B-4D59-AFE6-CB9D24DA30C0
rank
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type
BestRank
Statement
wasDerivedFrom
c64c66a34f560799ef9f089dd549623bea6bbdeb
P2860
Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene