Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion> ?p ?o ?g. }
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- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion type Assertion NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_head.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion wasGeneratedBy ECO_0000203 NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion wasDerivedFrom befree-2016 NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion SIO_000772 18195150 NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion evidence source_evidence_literature NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion description "[Although we initially focused on the mutation in POLG2, the mutation in OPA1 is more likely to explain the late-onset PEO and multisystem disorder in this patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.