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Q24295035-F927F493-0410-48F9-90E1-9BCC6EC1584C
Q24295035-F927F493-0410-48F9-90E1-9BCC6EC1584C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24295035-F927F493-0410-48F9-90E1-9BCC6EC1584C
Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis
P921
Q24295035-F927F493-0410-48F9-90E1-9BCC6EC1584C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24295035-F927F493-0410-48F9-90E1-9BCC6EC1584C
rank
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type
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Statement
wasDerivedFrom
17da9be1f8890cd10616e848aec6b571eb80d078
P921
Notch receptor 2