Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_assertion type Assertion NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_head.
- NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_assertion wasGeneratedBy ECO_0000203 NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_provenance.
- NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_assertion wasDerivedFrom befree-20140225 NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_provenance.
- NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_assertion SIO_000772 18371931 NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_provenance.
- NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_assertion evidence source_evidence_literature NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_provenance.
- NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_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." NP584216.RABDmTYSaeABgfg64PKpVKmoVLorA0anKeQSvvFwJbX0g130_provenance.