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- NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_assertion type Assertion NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_head.
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- NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_assertion wasDerivedFrom befree-2016 NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_provenance.
- NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_assertion SIO_000772 12873860 NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_provenance.
- NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_assertion evidence source_evidence_literature NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_provenance.
- NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_assertion description "[Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP402611.RA5tEXHV3XVUZNvjRt5J3sEZsBNmOsBFnjNJoaMThJ7Gs130_provenance.