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- NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_assertion type Assertion NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_head.
- NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_assertion wasGeneratedBy ECO_0000203 NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_provenance.
- NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_assertion wasDerivedFrom befree-20140225 NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_provenance.
- NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_assertion SIO_000772 8027054 NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_provenance.
- NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_assertion evidence source_evidence_literature NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_provenance.
- NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_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." NP643245.RAmXQrghSJJjNhXGvlbrfxKWw5yRc25v2G0QqA2a0H4ZA130_provenance.