Matches in Nanopublications for { ?s ?p "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625881.RAqazs6whC5Vv-Urqjs_30GfMfhl_P8AbCN6K8la9hl4Q130_provenance.
- NP469108.RAkvLLVwoE5QIsqg6O_fTnxv3QzmEZcaGOebA0yi0RwZY130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469108.RAkvLLVwoE5QIsqg6O_fTnxv3QzmEZcaGOebA0yi0RwZY130_provenance.
- NP500716.RAbye3UF8RqfJjEQrcGvn6H-GmundkfSda_tU8X6MQJB8130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500716.RAbye3UF8RqfJjEQrcGvn6H-GmundkfSda_tU8X6MQJB8130_provenance.
- NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420802.RAVmkGt-pq5LSbJ8KJXM_iW-bLc7grsz3jjP4hpR0Q-U4130_provenance.
- assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP824102.RAlHarMGyolz4UPbnbwKIadWsaR9K8-J6c6XnfA2Jsvwg130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824102.RAlHarMGyolz4UPbnbwKIadWsaR9K8-J6c6XnfA2Jsvwg130_provenance.
- NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824112.RAIO3DwK8i-Ml4UUcDeru7KcTa6gk0iTZzSvkmuZb3Kx8130_provenance.
- NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1085256.RAGUU72wWmwYeQe_cXVrx2yo-io383E3ZLhudemUCqU2o130_provenance.
- NP1085257.RAHe_5riRNPIliFDwOwfpBhIztblHrE5lIsYr0YTsma4E130_assertion description "[Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1085257.RAHe_5riRNPIliFDwOwfpBhIztblHrE5lIsYr0YTsma4E130_provenance.