Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP614118.RACVsM1dfCFChgH5sdq8h3Vjf1XGuXinknXdkGmcalABE130_provenance.