Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_assertion> ?p ?o ?g. }
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- NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_assertion type Assertion NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_head.
- NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_assertion wasGeneratedBy ECO_0000203 NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_provenance.
- NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_assertion wasDerivedFrom befree-20140225 NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_provenance.
- NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_assertion SIO_000772 22215554 NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_provenance.
- NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_assertion evidence source_evidence_literature NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_provenance.
- NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_assertion description "[There are a set of recurrent point mutations in the mitochondrial DNA (mtDNA) that are responsible for common mitochondrial diseases, including MELAS (mitochondrial encephalopathy, lactic acidosis, stroke-like episodes), MERRF (myoclonic epilepsy and ragged red fibers), LHON (Leber's hereditary optic neuropathy), NARP (neuropathy, ataxia, retinitis pigmentosa), and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580768.RAUy3Y9fEfvZHYahjoa5StN6LX3cnpNLwYVXfOC9w1JeE130_provenance.