Matches in Wikidata for { <http://www.wikidata.org/entity/Q55788117> ?p ?o ?g. }
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- Q55788117 description "human disease" @default.
- Q55788117 description "хвороба людини" @default.
- Q55788117 name "autosomal recessive severe congenital neutropenia due to CXCR2 deficiency" @default.
- Q55788117 type Item @default.
- Q55788117 label "autosomal recessive severe congenital neutropenia due to CXCR2 deficiency" @default.
- Q55788117 prefLabel "autosomal recessive severe congenital neutropenia due to CXCR2 deficiency" @default.
- Q55788117 P1550 Q55788117-6F36D29D-E8B5-490D-9745-0DA237F9A30D @default.
- Q55788117 P279 Q55788117-cb4a7b30-4bb4-8f2c-1146-aa6ab802ad9f @default.
- Q55788117 P2888 Q55788117-332E1BC4-5DE4-447C-98F9-ACA2AAE48498 @default.
- Q55788117 P31 Q55788117-310BFC35-ACE9-4048-A975-61512222F703 @default.
- Q55788117 P4229 Q55788117-EEBBC8C6-57A3-4D5A-8D44-ABB1E46B39FC @default.
- Q55788117 P5270 Q55788117-E1330BDA-D015-4B8B-8C97-6ED047BD9224 @default.
- Q55788117 P5270 MONDO_0018487 @default.
- Q55788117 P1550 "420699" @default.
- Q55788117 P279 Q18553325 @default.
- Q55788117 P2888 Orphanet_420699 @default.
- Q55788117 P31 Q112193867 @default.
- Q55788117 P4229 "D70" @default.
- Q55788117 P5270 "MONDO_0018487" @default.