Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion> ?p ?o ?g. }
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- NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion type Assertion NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_head.
- NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion description "[We performed direct genotyping of INF2 in 16 index patients with Charcot-Marie-Tooth neuropathy and FSGS who did not have a mutation in PMP22 or MPZ, encoding peripheral myelin protein 22 and myelin protein zero, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_provenance.
- NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion evidence source_evidence_literature NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_provenance.
- NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion SIO_000772 22187985 NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_provenance.
- NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion wasDerivedFrom befree-2016 NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_provenance.
- NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_assertion wasGeneratedBy ECO_0000203 NP948368.RA25v5WvxentnfSvJYyH3Hj9oi5SofcVjZC4Y_e3AcrNU130_provenance.