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- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion type Assertion NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_head.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion wasGeneratedBy ECO_0000203 NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion wasDerivedFrom befree-20150227 NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion SIO_000772 15863660 NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion evidence source_evidence_literature NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.
- NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_assertion description "[Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP323399.RAReez8fLWbtLI8yb1bG4EuJl7ImwATU7I_l-cf-Qbvr0130_provenance.