Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP379609.RAAQEyPAWQd4cWyo2srCDHFSDtGWWkYpwugNiUy7sNqOQ130_provenance.