Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_assertion type Assertion NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_head.
- NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_assertion description "[Mutations in the chloride channel gene, CLCNKB, usually cause classic Bartter syndrome (cBS) or a mixed Bartter-Gitelman phenotype in the first years of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.
- NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_assertion evidence source_evidence_literature NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.
- NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_assertion SIO_000772 16391491 NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.
- NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_assertion wasDerivedFrom befree-20140225 NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.
- NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_assertion wasGeneratedBy ECO_0000203 NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.