Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_assertion> ?p ?o ?g. }
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- NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_assertion type Assertion NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_head.
- NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_assertion wasGeneratedBy ECO_0000203 NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_provenance.
- NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_assertion wasDerivedFrom befree-2016 NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_provenance.
- NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_assertion SIO_000772 16258268 NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_provenance.
- NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_assertion evidence source_evidence_literature NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_provenance.
- NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_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." NP520262.RAkFGUTwLdFW9ge_yREFXToN6GSUbqM-aClisYjDzOuuM130_provenance.