Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_assertion> ?p ?o ?g. }
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- NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_assertion type Assertion NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_head.
- NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_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." NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_provenance.
- NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_assertion evidence source_evidence_literature NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_provenance.
- NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_assertion SIO_000772 16645216 NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_provenance.
- NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_assertion wasDerivedFrom befree-20140225 NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_provenance.
- NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_assertion wasGeneratedBy ECO_0000203 NP483022.RAPk0284hVi3JF5S3xZQamrORK_HOf0rf_ABK2a9m_FRU130_provenance.