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Q48035493-33CC7949-80A8-4EB1-8D1E-B622F27634E6
Q48035493-33CC7949-80A8-4EB1-8D1E-B622F27634E6
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Statement
http://www.wikidata.org/entity/statement/Q48035493-33CC7949-80A8-4EB1-8D1E-B622F27634E6
Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes.
P2860
Q48035493-33CC7949-80A8-4EB1-8D1E-B622F27634E6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48035493-33CC7949-80A8-4EB1-8D1E-B622F27634E6
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wasDerivedFrom
c25fb7d7157f87c26d8b790b7a1cc8f2f89c89b8
P2860
Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster