Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_assertion> ?p ?o ?g. }
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- NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_assertion type Assertion NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_head.
- NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_assertion description "[The 3243A>G mutation in the MTTL1 (tRNA(Leu)) gene and the 8344A>G mutation in the MTTK (tRNA(Lys)) gene are the most common mutations found in mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes and myoclonic epilepsy associated with ragged-red fibers, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_provenance.
- NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_assertion evidence source_evidence_literature NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_provenance.
- NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_assertion SIO_000772 16645216 NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_provenance.
- NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_assertion wasDerivedFrom befree-2016 NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_provenance.
- NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_assertion wasGeneratedBy ECO_0000203 NP547284.RAQiRgIx8h2LQRE2N9_YRB6taz6g3RdcqveOV3R_ACDRE130_provenance.