Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1235346.RAqevmM0pynvRIih5-MZbH5D8X-NjEPxmGVTB_iJsiR-s130_provenance.