Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP914256.RAjvUvfU7HdX5mO77T_OKnO_eXriBdbJ_VA9eYfQHd7LA130_provenance.