Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_assertion> ?p ?o ?g. }
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- NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_assertion type Assertion NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_head.
- NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_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." NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_provenance.
- NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_assertion evidence source_evidence_literature NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_provenance.
- NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_assertion SIO_000772 19845429 NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_provenance.
- NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_assertion wasDerivedFrom befree-2016 NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_provenance.
- NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_assertion wasGeneratedBy ECO_0000203 NP770719.RAzz0bk9tQnbvzggEdBcdgGXRBt7EX3VN19XtY_KyRLZA130_provenance.