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Q24676539-30D6042A-D73F-4CCA-8217-61B5FE42868D
Q24676539-30D6042A-D73F-4CCA-8217-61B5FE42868D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676539-30D6042A-D73F-4CCA-8217-61B5FE42868D
Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms
P932
Q24676539-30D6042A-D73F-4CCA-8217-61B5FE42868D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676539-30D6042A-D73F-4CCA-8217-61B5FE42868D
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
a4037ca3ada04d92b55cb1badb2a7e02d0b5625f
P932
1735560
http://www.w3.org/2001/XMLSchema#string