Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_assertion> ?p ?o ?g. }
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- NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_assertion type Assertion NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_head.
- NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_assertion wasGeneratedBy ECO_0000203 NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_assertion wasDerivedFrom befree-2016 NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_assertion SIO_000772 17141632 NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_assertion evidence source_evidence_literature NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_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.