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- NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_assertion type Assertion NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_head.
- NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_assertion wasGeneratedBy ECO_0000203 NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_provenance.
- NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_assertion wasDerivedFrom befree-20140225 NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_provenance.
- NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_assertion SIO_000772 10359058 NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_provenance.
- NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_assertion evidence source_evidence_literature NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_provenance.
- NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_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." NP723496.RANZ_nov0gbrC3gL6y0gnOJOZoAutSAm33iKhfOVZuef0130_provenance.