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Q24293498-6CBBF7F4-BA97-4DC4-B4E5-DFAD5F15F4C2
Q24293498-6CBBF7F4-BA97-4DC4-B4E5-DFAD5F15F4C2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24293498-6CBBF7F4-BA97-4DC4-B4E5-DFAD5F15F4C2
NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway
P2860
Q24293498-6CBBF7F4-BA97-4DC4-B4E5-DFAD5F15F4C2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24293498-6CBBF7F4-BA97-4DC4-B4E5-DFAD5F15F4C2
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type
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wasDerivedFrom
1f744fc72052562643e6292321cdcc70a7437a83
P2860
Notch signaling and inherited disease syndromes.