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- NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_assertion type Assertion NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_head.
- NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_assertion wasGeneratedBy ECO_0000203 NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_provenance.
- NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_assertion wasDerivedFrom befree-2016 NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_provenance.
- NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_assertion SIO_000772 10359058 NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_provenance.
- NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_assertion evidence source_evidence_literature NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_provenance.
- NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_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." NP254077.RAP1qiX6Mt6p-OWVTG6zFs2V1gKYEexgCsKUJ6QmKNsEg130_provenance.