Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_assertion wasGeneratedBy ECO_0000203 NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_assertion wasDerivedFrom befree-20140225 NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_assertion SIO_000772 16258268 NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_assertion evidence source_evidence_literature NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_assertion description "[Natural p63 mutants, associated to the AEC syndrome, show a partial or complete lack of transactivation potential of the p57Kip2 promoter, while three other natural p63 mutants, associated to the EEC, LMS and SHFM-4 syndromes, were less affected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP355262.RAXlJWOMbO-jC4cTv2qo_cilh9lALHAsW3G35uW0M0EDc130_provenance.