Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion type Assertion NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_head.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion description "[Gain-of-function mutations in TRPC6 cause hereditary focal segmental glomerulosclerosis (FSGS), and several human acquired proteinuric diseases show increased glomerular TRPC6 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion evidence source_evidence_literature NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion SIO_000772 21839714 NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion wasDerivedFrom befree-2016 NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.
- NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_assertion wasGeneratedBy ECO_0000203 NP916867.RAauj061HaOQIU5iay-TnWD2apoWz44NafhGf9ejleeow130_provenance.