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- NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_assertion type Assertion NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_head.
- NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_assertion description "[Crigler-Najjar syndrome (CNS), caused by deficiency of bilirubin uridine diphosphate glucuronosyltransferase (UGT) 1A1, is a rare and autosomal recessive inherited disorder characterized by severe unconjugated nonhemolytic hyperbilirubinemia since birth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_provenance.
- NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_assertion evidence source_evidence_literature NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_provenance.
- NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_assertion SIO_000772 24341141 NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_provenance.
- NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_assertion wasDerivedFrom befree-20140225 NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_provenance.
- NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_assertion wasGeneratedBy ECO_0000203 NP661030.RAyZB_hnEO9MfKZ1g8rdzJBfNsjH65seJ4MwlThmOZlps130_provenance.