Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_assertion type Assertion NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_head.
- NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_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." NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_provenance.
- NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_assertion evidence source_evidence_literature NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_provenance.
- NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_assertion SIO_000772 10802646 NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_provenance.
- NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_assertion wasDerivedFrom befree-20140225 NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_provenance.
- NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_assertion wasGeneratedBy ECO_0000203 NP718709.RAsQ8r7dyR6meMeu5QgDaR0wP2QzylLHhbabWm4E5Uyg0130_provenance.