Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_assertion> ?p ?o ?g. }
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- NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_assertion type Assertion NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_head.
- NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_assertion description "[Moreover, EMSA and ChIP assays demonstrated that the allele A disrupts the binding site of ETS-1, thus markedly decreases the activity of the TBX22 promoter, which is likely to lead to the birth defect of the CPO without ankyloglossia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.
- NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_assertion evidence source_evidence_literature NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.
- NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_assertion SIO_000772 25373698 NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.
- NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_assertion wasDerivedFrom befree-2016 NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.
- NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_assertion wasGeneratedBy ECO_0000203 NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.