Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_assertion type Assertion NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_head.
- NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_assertion description "[Overall, two distinct and novel RyR2 mutations were identified in two cases of SIDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.
- NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_assertion evidence source_evidence_literature NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.
- NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_assertion SIO_000772 17556193 NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.
- NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_assertion wasDerivedFrom befree-2016 NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.
- NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_assertion wasGeneratedBy ECO_0000203 NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.