Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_assertion> ?p ?o ?g. }
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- NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_assertion type Assertion NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_head.
- NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_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." NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_provenance.
- NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_assertion evidence source_evidence_literature NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_provenance.
- NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_assertion SIO_000772 18195150 NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_provenance.
- NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_assertion wasDerivedFrom befree-2016 NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_provenance.
- NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_assertion wasGeneratedBy ECO_0000203 NP649937.RAvNdf37893UTCUA3dEKvUFnoPTvK8yzXt5hIKJwQI7Po130_provenance.