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- Q74193859 description "artículu científicu espublizáu en xunetu de 2000" @default.
- Q74193859 description "im Juli 2000 veröffentlichter wissenschaftlicher Artikel" @default.
- Q74193859 description "scientific article published on 01 July 2000" @default.
- Q74193859 description "wetenschappelijk artikel" @default.
- Q74193859 description "наукова стаття, опублікована в липні 2000" @default.
- Q74193859 name "[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]" @default.
- Q74193859 name "[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]" @default.
- Q74193859 type Item @default.
- Q74193859 label "[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]" @default.
- Q74193859 label "[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]" @default.
- Q74193859 prefLabel "[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]" @default.
- Q74193859 prefLabel "[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]" @default.
- Q74193859 P1433 Q74193859-80785F47-05C3-4967-A19C-3FDD27F46EDD @default.
- Q74193859 P1476 Q74193859-758D1A90-A0FC-4948-A785-E0575ACD227F @default.
- Q74193859 P2093 Q74193859-1D6FC0BB-48EC-4EAE-B537-DC145E3031F5 @default.
- Q74193859 P2093 Q74193859-3FDF02CE-D4B2-4DF7-B17A-A368AE7D138C @default.
- Q74193859 P2093 Q74193859-40A134B2-2554-48B5-9C39-F47868F6867B @default.
- Q74193859 P2093 Q74193859-442F2F21-572B-48FE-8301-F98FF747E85F @default.
- Q74193859 P2093 Q74193859-94C44A1E-2137-433A-9254-AC6CCA4BD79D @default.
- Q74193859 P2093 Q74193859-98FC310D-B873-453F-A1B2-7DACF15F5EEB @default.
- Q74193859 P304 Q74193859-A8FBCD41-D8C7-4FB3-93FF-6B629852617A @default.
- Q74193859 P31 Q74193859-920093cc-151e-4eba-bd8e-60431658ecad @default.
- Q74193859 P31 Q74193859-D853C696-1EB8-4009-8EF4-1950411A924E @default.
- Q74193859 P356 Q74193859-D0EDD0BF-3383-4B8F-B7E7-86179E91AEAD @default.
- Q74193859 P433 Q74193859-D5AD76C8-871F-4459-9B62-1369F12610AC @default.
- Q74193859 P478 Q74193859-64A8E5C1-8F51-4B65-BF25-83ED42E0F655 @default.
- Q74193859 P577 Q74193859-37797158-1E77-4BB3-ADC2-330BBF3E6430 @default.
- Q74193859 P698 Q74193859-F169BC66-90FC-4872-84E8-7F453BDDC863 @default.
- Q74193859 P921 Q74193859-05BDCDC9-5F77-45AE-8ACA-460B12FDF8F3 @default.
- Q74193859 P356 S-2000-10382 @default.
- Q74193859 P698 10949816 @default.
- Q74193859 P1433 Q15767651 @default.
- Q74193859 P1476 "[Mutations in the keratin gene as a cause of Meesman-Wilke corneal dystrophy and autosomal dominant skin cornification disorders]" @default.
- Q74193859 P2093 "Nölle B" @default.
- Q74193859 P2093 "Rochels R" @default.
- Q74193859 P2093 "Swensson B" @default.
- Q74193859 P2093 "Swensson O" @default.
- Q74193859 P2093 "Thiel HJ" @default.
- Q74193859 P2093 "Wannke B" @default.
- Q74193859 P304 "43-51" @default.
- Q74193859 P31 Q13442814 @default.
- Q74193859 P31 Q7318358 @default.
- Q74193859 P356 "10.1055/S-2000-10382" @default.
- Q74193859 P433 "1" @default.
- Q74193859 P478 "217" @default.
- Q74193859 P577 "2000-07-01T00:00:00Z" @default.
- Q74193859 P698 "10949816" @default.
- Q74193859 P921 Q2044949 @default.