Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_assertion> ?p ?o ?g. }
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- NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_assertion type Assertion NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_head.
- NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_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." NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_provenance.
- NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_assertion evidence source_evidence_literature NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_provenance.
- NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_assertion SIO_000772 18195150 NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_provenance.
- NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_assertion wasDerivedFrom befree-2016 NP649936.RAP5kM-4VqPYF7YgR173kif06Y2VeGtuo7adwmQDkUBSk130_provenance.
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