Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_assertion> ?p ?o ?g. }
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- NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_assertion type Assertion NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_head.
- NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_assertion wasGeneratedBy ECO_0000203 NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_provenance.
- NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_assertion wasDerivedFrom befree-20140225 NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_provenance.
- NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_assertion SIO_000772 17141632 NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_provenance.
- NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_assertion evidence source_evidence_literature NP671904.RARoUdKuCYIRdSTxk1KSDV1NgPLwB_CsH35RyUeiFxDtc130_provenance.
- 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.