Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_assertion> ?p ?o ?g. }
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- NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_assertion type Assertion NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_head.
- NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_assertion wasGeneratedBy ECO_0000203 NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_provenance.
- NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_assertion wasDerivedFrom befree-20140225 NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_provenance.
- NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_assertion SIO_000772 18806273 NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_provenance.
- NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_assertion evidence source_evidence_literature NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_provenance.
- NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_assertion description "[Leber's hereditary optic neuropathy (LHON), the most frequent mitochondrial disorder, is mostly due to three mitochondrial DNA (mtDNA) mutations in respiratory chain complex I subunit genes: 3460/ND1, 11778/ND4 and 14484/ND6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212989.RApm7dnjItyYhKsyBH6iPHAVLQohnAj-G0HvelJSaRoNY130_provenance.