Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP626517.RAax76UN82MGiLQjEYbF50A72sY1OSmMxFb9_wY4w4PRA130_provenance.