Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- befree-2016 importedOn "2016-02-19" NP582042.RAxCcZEjWQxnDGf2Xq2WUpSMY-36EVINqJwKvfhHpPNfI130_provenance.
- 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.