Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_assertion type Assertion NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_head.
- NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_assertion description "[consistent with recent findings of defects in the homologous cmoat gene in two rat models of hyperbilirubinemia (TR- and Eisai), we report two deletions and a missense mutation in the active transport family signature region in the gene in patients with hyperbilirubinemia II/Dubin-Johnson syndrome (DJS; MIM 237500), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_provenance.
- NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_assertion evidence source_evidence_literature NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_provenance.
- NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_assertion SIO_000772 9425227 NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_provenance.
- NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_assertion wasDerivedFrom befree-20150227 NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_provenance.
- NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_assertion wasGeneratedBy ECO_0000203 NP318176.RAb2sQophY0GhRj8y4wURA6shtryn_OER5EGcOdLHJdiM130_provenance.