Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion type Assertion NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_head.
- NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion description "[The archetypal NARP syndrome is almost exclusively associated with the m.8993T>C/G mutation in the sixth subunit of the mitochondrial ATP synthase, whereas other mutations in the MT-ATP6 gene primarily associate with Leigh syndrome or Leber's hereditary optic neuropathy (LHON).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_provenance.
- NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion evidence source_evidence_literature NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_provenance.
- NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion SIO_000772 23266623 NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_provenance.
- NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion wasDerivedFrom befree-20140225 NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_provenance.
- NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_assertion wasGeneratedBy ECO_0000203 NP692116.RAYd8WTkPIL12I3R6BFybSQ-noL2Q9kvB5wUvj8NlPhwU130_provenance.