Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_assertion type Assertion NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_head.
- NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_assertion description "[The results support the concept that deletions as well as depletion of mtDNA are involved in the pathogenesis of Alpers-Huttenlocher syndrome and add 3 new POLG1 mutations associated with an early-onset neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_provenance.
- NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_assertion evidence source_evidence_literature NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_provenance.
- NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_assertion SIO_000772 16896309 NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_provenance.
- NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_assertion wasDerivedFrom befree-2016 NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_provenance.
- NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_assertion wasGeneratedBy ECO_0000203 NP563379.RA9hIfAI-mUYn1nFZZiyhybvumcu7X-ayz4-ABNUYpSHQ130_provenance.