Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the 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.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion evidence source_evidence_literature NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion SIO_000772 18195150 NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion wasDerivedFrom befree-2016 NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_assertion wasGeneratedBy ECO_0000203 NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.
- befree-2016 importedOn "2016-02-19" NP649942.RA5y7J6IJj0ERK4ZalZRQgDvMm1B8jJHoxT2v8PmUCDmU130_provenance.