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- NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_assertion type Assertion NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_head.
- NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_assertion wasGeneratedBy ECO_0000203 NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_provenance.
- NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_assertion wasDerivedFrom befree-20150227 NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_provenance.
- NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_assertion SIO_000772 8027054 NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_provenance.
- NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_assertion evidence source_evidence_literature NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_provenance.
- NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_assertion description "[Crigler-Najjar syndrome type I (CN-I) is caused by an inherited absence of UDP-glucuronosyltransferase activity toward bilirubin (B-UGT), resulting in severe non-hemolytic unconjugated hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766316.RAetac0kmCqCXSgtOfB-kMa2xcCVW7OYpqKuJXOjVly_A130_provenance.