Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_assertion wasGeneratedBy ECO_0000203 NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_assertion wasDerivedFrom befree-20150227 NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_assertion SIO_000772 15148291 NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_assertion evidence source_evidence_literature NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.
- NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_assertion description "[Loss-of-function mutations of ClC-Kb lead to classic Bartter syndrome, a rare salt-wasting disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315502.RAFSUZthFMk2gmp6wPSsTZgL_lKmLIi6vPwUh0NBrtCUs130_provenance.