Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_assertion> ?p ?o ?g. }
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- NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_assertion type Assertion NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_head.
- NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_assertion wasGeneratedBy ECO_0000203 NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_assertion wasDerivedFrom befree-20150227 NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_assertion SIO_000772 10359058 NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_assertion evidence source_evidence_literature NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_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." NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.