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- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion type Assertion NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_head.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion wasGeneratedBy ECO_0000203 NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion wasDerivedFrom befree-20150227 NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion SIO_000772 10359058 NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_assertion evidence source_evidence_literature NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.
- NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_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." NP793421.RAP8lKKGDVL-FNBwDdGX7a_c0zxGl3pvsTMWkmcI9sSL8130_provenance.