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- NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_assertion type Assertion NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_head.
- NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_assertion wasGeneratedBy ECO_0000203 NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_provenance.
- NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_assertion wasDerivedFrom befree-20150227 NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_provenance.
- NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_assertion SIO_000772 10359058 NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_provenance.
- NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_assertion evidence source_evidence_literature NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_provenance.
- NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_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." NP912694.RAFX7k7Ho-Rn3UZ9MZk58IVJ4KyuHOHYHDHEk4l5kudSs130_provenance.