Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion type Assertion NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_head.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_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." NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion evidence source_evidence_literature NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion SIO_000772 24341141 NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion wasDerivedFrom befree-20140225 NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.
- NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_assertion wasGeneratedBy ECO_0000203 NP717684.RAXHUGy24GTZglYTRm10Pq0QLr_b_npSBjwhUhGg-sdOs130_provenance.