Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_assertion> ?p ?o ?g. }
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- NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_assertion type Assertion NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_head.
- NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_assertion description "[Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_provenance.
- NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_assertion evidence source_evidence_curated NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_provenance.
- NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_assertion SIO_000772 12761627 NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_provenance.
- NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_assertion wasDerivedFrom uniprot-2016 NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_provenance.
- NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_assertion wasGeneratedBy ECO_0000218 NP2697.RAbqktoVZGAEpU_N_jQiGpgNtc0i_wKs24wRqS3WHJERk130_provenance.