Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_assertion type Assertion NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_head.
- NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_assertion description "[Dominantly inherited cataracts with differing clinical features were found in two families carrying different point mutations in the gene encoding lens water channel protein AQP0 (major intrinsic protein, MIP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_provenance.
- NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_assertion evidence source_evidence_literature NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_provenance.
- NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_assertion SIO_000772 11001937 NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_provenance.
- NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_assertion wasDerivedFrom befree-2016 NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_provenance.
- NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_assertion wasGeneratedBy ECO_0000203 NP295874.RArqWYWqJPkZcnvm6faN6Fll0J9O1l174XjoAPhZ-Wx-s130_provenance.