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Q38110760-9238297C-0E20-4DFB-98F3-DAFFF82E9931
Q38110760-9238297C-0E20-4DFB-98F3-DAFFF82E9931
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38110760-9238297C-0E20-4DFB-98F3-DAFFF82E9931
Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.
P2860
Q38110760-9238297C-0E20-4DFB-98F3-DAFFF82E9931
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38110760-9238297C-0E20-4DFB-98F3-DAFFF82E9931
rank
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Statement
wasDerivedFrom
a40793129c56d090d76cf37665f55f36273ee5ae
P2860
The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region