Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_assertion> ?p ?o ?g. }
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- NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_assertion type Assertion NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_head.
- NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_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." NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_provenance.
- NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_assertion evidence source_evidence_literature NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_provenance.
- NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_assertion SIO_000772 9539740 NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_provenance.
- NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_assertion wasDerivedFrom befree-2016 NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_provenance.
- NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_assertion wasGeneratedBy ECO_0000203 NP1392748.RA6_Y6KqUuEnwOO9E6C9NH3hz5eCuJGUMjpGLwKviEp6I130_provenance.