Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_assertion type Assertion NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_head.
- NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_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." NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.
- NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_assertion evidence source_evidence_literature NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.
- NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_assertion SIO_000772 21810944 NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.
- NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_assertion wasDerivedFrom befree-2016 NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.
- NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_assertion wasGeneratedBy ECO_0000203 NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.