Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_assertion type Assertion NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_head.
- NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_assertion description "[Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_provenance.
- NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_assertion evidence source_evidence_curated NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_provenance.
- NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_assertion SIO_000772 9539740 NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_provenance.
- NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_assertion wasDerivedFrom ctd_human-2016 NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_provenance.
- NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_assertion wasGeneratedBy ECO_0000218 NP37792.RAFSUumDG4PP1jClWFQchiSqhDg0TGCYqgof0id7LhD8Q130_provenance.