Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion type Assertion NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_head.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion description "[Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion evidence source_evidence_literature NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion SIO_000772 10802646 NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion wasDerivedFrom befree-20150227 NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion wasGeneratedBy ECO_0000203 NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.