Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion type Assertion NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_head.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion description "[? The UGT1A1 211G>A mutation is associated with neonatal hyperbilirubinemia in Asians, but not in Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion evidence source_evidence_literature NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion SIO_000772 21272068 NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion wasDerivedFrom befree-2016 NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.
- NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_assertion wasGeneratedBy ECO_0000203 NP868198.RA8L6l-aRn0DG9zMsmH_yPyqqIfyNK1NHIbf0hW4cu-mk130_provenance.