Matches in Nanopublications for { ?s ?p "[Mutations in PERK (EIF2AK3) result in permanent neonatal diabetes as well as several other anomalies that underlie the human Wolcott-Rallison syndrome, and these anomalies are mirrored in Perk knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_assertion description "[Mutations in PERK (EIF2AK3) result in permanent neonatal diabetes as well as several other anomalies that underlie the human Wolcott-Rallison syndrome, and these anomalies are mirrored in Perk knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_provenance.
- NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_assertion description "[Mutations in PERK (EIF2AK3) result in permanent neonatal diabetes as well as several other anomalies that underlie the human Wolcott-Rallison syndrome, and these anomalies are mirrored in Perk knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824098.RA2ek7NRFHW4NF8FpfY4mIAkDZsL-pslfDid-XwufGw2k130_provenance.
- NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_assertion description "[Mutations in PERK (EIF2AK3) result in permanent neonatal diabetes as well as several other anomalies that underlie the human Wolcott-Rallison syndrome, and these anomalies are mirrored in Perk knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- NP582041.RARD9YO3qJVorRp1FcBWMEuN1wehSdGI49GlUdkr-PYnE130_assertion description "[Mutations in PERK (EIF2AK3) result in permanent neonatal diabetes as well as several other anomalies that underlie the human Wolcott-Rallison syndrome, and these anomalies are mirrored in Perk knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582041.RARD9YO3qJVorRp1FcBWMEuN1wehSdGI49GlUdkr-PYnE130_provenance.
- assertion description "[Mutations in PERK (EIF2AK3) result in permanent neonatal diabetes as well as several other anomalies that underlie the human Wolcott-Rallison syndrome, and these anomalies are mirrored in Perk knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.