Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_assertion> ?p ?o ?g. }
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- NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_assertion type Assertion NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_head.
- NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_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." NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_provenance.
- NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_assertion evidence source_evidence_literature NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_provenance.
- NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_assertion SIO_000772 11001937 NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_provenance.
- NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_assertion wasDerivedFrom befree-20150227 NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_provenance.
- NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_assertion wasGeneratedBy ECO_0000203 NP527020.RAT3CakYBxr3HgmnYAvVbMqw5oXaAqYE4SmustaWkno5s130_provenance.