Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_assertion> ?p ?o ?g. }
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- NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_assertion type Assertion NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_head.
- NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_assertion description "[This review highlights the major clinical features of both Gilbert's Syndrome and G-6-PD deficiency, and surveys a series of studies related to neonatal jaundice in G-6-PD-deficient neonates culminating in the documentation of an interaction between the two conditions that is crucial to the pathogenesis of hyperbilirubinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_provenance.
- NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_assertion evidence source_evidence_literature NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_provenance.
- NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_assertion SIO_000772 11803413 NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_provenance.
- NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_assertion wasDerivedFrom befree-20150227 NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_provenance.
- NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_assertion wasGeneratedBy ECO_0000203 NP415478.RAeyCUA-HFXjs8cBL2AtOIOl7nBZW_jslKE5C2WJcWoO4130_provenance.