Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_assertion type Assertion NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_head.
- NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_assertion description "[Now, examination of the UGT1 gene structure in hyperbilirubinemic patients has revealed more than 100 different genetic defects in Crigler-Najjar syndromes and one genetic alternation that accounts for the majority of Gilbert's syndrome cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_provenance.
- NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_assertion evidence source_evidence_literature NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_provenance.
- NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_assertion SIO_000772 19845429 NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_provenance.
- NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_assertion wasDerivedFrom befree-20150227 NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_provenance.
- NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_assertion wasGeneratedBy ECO_0000203 NP912421.RAw7yXWo51EEzOTCGe9eXqdRUt9-q7FqtgyX4C78YxBUY130_provenance.