Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_assertion> ?p ?o ?g. }
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- NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_assertion type Assertion NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_head.
- NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_assertion description "[The R91P mutant identified in Axenfeld Rieger syndrome is a dominant-negative factor, which is able to block the expression of several pituitary genes activated by PITX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.
- NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_assertion evidence source_evidence_literature NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.
- NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_assertion SIO_000772 21810944 NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.
- NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_assertion wasDerivedFrom befree-20150227 NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.
- NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_assertion wasGeneratedBy ECO_0000203 NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.