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Q30492620-D12FCB0C-89A0-4663-B46C-A0AC435B68DB
Q30492620-D12FCB0C-89A0-4663-B46C-A0AC435B68DB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30492620-D12FCB0C-89A0-4663-B46C-A0AC435B68DB
A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.
P5875
Q30492620-D12FCB0C-89A0-4663-B46C-A0AC435B68DB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30492620-D12FCB0C-89A0-4663-B46C-A0AC435B68DB
rank
NormalRank
type
BestRank
Statement
P5875
38059095
http://www.w3.org/2001/XMLSchema#string