Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_assertion type Assertion NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_head.
- NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_assertion description "[The ND1 subunit gene of the mitochondrial NADH-ubiquinone oxidoreductase (complex I) is a hot spot for mutations causing Leber hereditary optic neuropathy and several mutations causing the mitochondrial encephalopathy, lactic acidosis and stroke-like episodes syndrome (MELAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_provenance.
- NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_assertion evidence source_evidence_literature NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_provenance.
- NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_assertion SIO_000772 16849371 NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_provenance.
- NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_assertion wasDerivedFrom befree-2016 NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_provenance.
- NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_assertion wasGeneratedBy ECO_0000203 NP560208.RAAQUp9VenJVKg2wQVVC6d8G_Xenx-I-BJNPw8joibRPQ130_provenance.