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- NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_assertion type Assertion NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_head.
- NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_assertion wasGeneratedBy ECO_0000203 NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_provenance.
- NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_assertion wasDerivedFrom gad-20150221 NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_provenance.
- NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_assertion SIO_000772 16557566 NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_provenance.
- NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_assertion evidence source_evidence_literature NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_provenance.
- NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_assertion description "[Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99628.RAMxu67WEBPgxYyJlB0km4W8185VsubzjZnFahffXe5P0130_provenance.