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Q51629774-2AEFC0C2-B87B-4298-A42B-0D3D6D6120F0
Q51629774-2AEFC0C2-B87B-4298-A42B-0D3D6D6120F0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51629774-2AEFC0C2-B87B-4298-A42B-0D3D6D6120F0
Muscle dysfunction caused by loss of Magel2 in a mouse model of Prader-Willi and Schaaf-Yang syndromes.
P2860
Q51629774-2AEFC0C2-B87B-4298-A42B-0D3D6D6120F0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51629774-2AEFC0C2-B87B-4298-A42B-0D3D6D6120F0
rank
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type
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Statement
wasDerivedFrom
1fcd33c96238dbe9695209d2e69d0ea4eeadbabc
P2860
The imprinted NPAP1/C15orf2 gene in the Prader-Willi syndrome region encodes a nuclear pore complex associated protein.