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- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion type Assertion NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_head.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion wasGeneratedBy ECO_0000203 NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion wasDerivedFrom befree-20150227 NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion SIO_000772 18195150 NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion evidence source_evidence_literature NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.
- NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_assertion description "[Although we initially focused on the mutation in POLG2, the mutation in OPA1 is more likely to explain the late-onset PEO and multisystem disorder in this patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP833587.RAw_W3wca2LvIAN8FAusw54w-11wVm8IjkFS4zejePF3k130_provenance.