Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_assertion> ?p ?o ?g. }
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- NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_assertion type Assertion NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_head.
- NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_assertion wasGeneratedBy ECO_0000203 NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_provenance.
- NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_assertion wasDerivedFrom befree-2016 NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_provenance.
- NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_assertion SIO_000772 8027054 NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_provenance.
- NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_assertion evidence source_evidence_literature NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_provenance.
- NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_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." NP1330198.RA3ORMJFZx1h425FtRAXNw-o0zjuK5FD4qjNfFKthoIVY130_provenance.