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- source_evidence_literature type ECO_0000212 NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- befree-20150227 importedOn "2015-02-27" NP766293.RABo0b8h6wp7neH1VntIa18nKp5XODPUmPWXFJmivz408130_provenance.
- 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.