Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_assertion type Assertion NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_head.
- NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_assertion description "[An XPB expression vector with the p.F99S mutation partially complemented the NER defect in XP-B cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_provenance.
- NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_assertion evidence source_evidence_curated NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_provenance.
- NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_assertion SIO_000772 16947863 NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_provenance.
- NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_assertion wasDerivedFrom uniprot-2016 NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_provenance.
- NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_assertion wasGeneratedBy ECO_0000218 NP4682.RA0dPdl9szBPm6bJgjic3s3gDzH1VM4V7J5pO8AqujNcc130_provenance.