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Q30492620-07F7CC3B-03EE-4B04-9A4E-46E8A4BDD322
Q30492620-07F7CC3B-03EE-4B04-9A4E-46E8A4BDD322
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30492620-07F7CC3B-03EE-4B04-9A4E-46E8A4BDD322
A novel form of cell type-specific partial IFN-gammaR1 deficiency caused by a germ line mutation of the IFNGR1 initiation codon.
P2093
Q30492620-07F7CC3B-03EE-4B04-9A4E-46E8A4BDD322
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30492620-07F7CC3B-03EE-4B04-9A4E-46E8A4BDD322
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
1b83765ca0674305ecbf324861610d4e64defa4c
P1545
12
http://www.w3.org/2001/XMLSchema#string
P2093
Ulla M Pihkala-Saarinen
http://www.w3.org/2001/XMLSchema#string