Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_assertion> ?p ?o ?g. }
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- NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_assertion type Assertion NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_head.
- NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_assertion description "[Whereas G-6-PD deficiency or Gilbert's Syndrome, alone, did not predispose to hyperbilirubinemia, G-6-PD-deficient neonates who also were heterozygotes or homozygotes for the variant UGT gene promoter did have significantly increased incidences of hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_provenance.
- NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_assertion evidence source_evidence_literature NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_provenance.
- NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_assertion SIO_000772 11803413 NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_provenance.
- NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_assertion wasDerivedFrom befree-20140225 NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_provenance.
- NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_assertion wasGeneratedBy ECO_0000203 NP500215.RAxGHRc3S53AaO3bOQtEGU3X5ZWsRo-K3kPNrlSOWGFEY130_provenance.