Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_assertion> ?p ?o ?g. }
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- NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_assertion type Assertion NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_head.
- NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_assertion wasGeneratedBy ECO_0000203 NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_provenance.
- NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_assertion wasDerivedFrom befree-20140225 NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_provenance.
- NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_assertion SIO_000772 18371931 NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_provenance.
- NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_assertion evidence source_evidence_literature NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_provenance.
- NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_assertion description "[We demonstrate that the pcy mutation generates a hypomorphic Nphp3 allele that is responsible for the cystic kidney disease phenotype, whereas complete loss of Nphp3 function results in situs inversus, congenital heart defects, and embryonic lethality in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP828799.RAP01jTWRc8SPbM0vnT7AHaOpXp5G5mtcBz6oLSvoueKk130_provenance.