Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- befree-2016 importedOn "2016-02-19" NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_assertion wasGeneratedBy ECO_0000203 NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_assertion wasDerivedFrom befree-2016 NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_assertion SIO_000772 16258268 NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_assertion evidence source_evidence_literature NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.
- NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_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." NP520263.RAvsTLZ5CE1_aqOEmOM--GD8LMzl1JwRkhbM_wdX8gFwE130_provenance.