Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_assertion> ?p ?o ?g. }
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- NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_assertion type Assertion NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_head.
- NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_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." NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_provenance.
- NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_assertion evidence source_evidence_literature NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_provenance.
- NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_assertion SIO_000772 11803413 NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_provenance.
- NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_assertion wasDerivedFrom befree-2016 NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_provenance.
- NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_assertion wasGeneratedBy ECO_0000203 NP342606.RAxAbsV6wrFU3NDiYT_kRLb0A0FUdPAJBsEqtBnmy-scc130_provenance.