Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_assertion> ?p ?o ?g. }
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- NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_assertion type Assertion NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_head.
- NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_assertion description "[A point mutation or a small deletion of mitochondrial DNA, probably affecting the COX-II gene, may be responsible for the COX deficiency in this case of MERRF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_provenance.
- NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_assertion evidence source_evidence_literature NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_provenance.
- NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_assertion SIO_000772 2549843 NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_provenance.
- NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_assertion wasDerivedFrom befree-2016 NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_provenance.
- NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_assertion wasGeneratedBy ECO_0000203 NP1247082.RATVGlFNTHnHu2qSZYjn552Dtckb0vHL8CA59CBYtFuDw130_provenance.