Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_assertion> ?p ?o ?g. }
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- NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_assertion type Assertion NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_head.
- NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_assertion wasGeneratedBy ECO_0000203 NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_provenance.
- NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_assertion wasDerivedFrom befree-2016 NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_provenance.
- NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_assertion SIO_000772 24262866 NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_provenance.
- NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_assertion evidence source_evidence_literature NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_provenance.
- NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_assertion description "[Mutation in the SURF1 is one of the most common nuclear mutations associated with Leigh syndrome and cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1130471.RARXjR2UcEamIg93_dUutMYNluAFiQMzggDD4X6dQTkyI130_provenance.