Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_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." NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_assertion evidence source_evidence_literature NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_assertion SIO_000772 11803413 NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_assertion wasDerivedFrom befree-20140225 NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_assertion wasGeneratedBy ECO_0000203 NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.
- befree-20140225 importedOn "2014-02-25" NP203262.RA1Ii_chvMEOQd-tcCZ2i995LQKiErX0Mi3MfNmKDiHao130_provenance.