Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_assertion type Assertion NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_head.
- NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_assertion wasGeneratedBy ECO_0000203 NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_provenance.
- NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_assertion wasDerivedFrom befree-2016 NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_provenance.
- NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_assertion SIO_000772 10359058 NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_provenance.
- NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_assertion evidence source_evidence_literature NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_provenance.
- NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_assertion description "[These findings imply a contribution of the UGT1A polymorphism associated to Gilbert's syndrome to development of the hyperbilirubinemia in G6PD deficient subjects during acute hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254081.RAAV73MssR28Nc8oGqkClhXM2jr4yzlSJ-O4aG44xiyWg130_provenance.