Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_assertion> ?p ?o ?g. }
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- NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_assertion type Assertion NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_head.
- NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_assertion wasGeneratedBy ECO_0000203 NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_provenance.
- NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_assertion wasDerivedFrom befree-2016 NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_provenance.
- NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_assertion SIO_000772 21615690 NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_provenance.
- NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_assertion evidence source_evidence_literature NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_provenance.
- NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_assertion description "[Several missense and heterozygous frame shift mutations, encoded within exon 13 and 14 of the p63 gene, have been identified in the p63α SAM domain in patients suffering from ankyloblepharon-ectodermal dysplasia-clefting syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897012.RAk4eY6S_jsfHfvS4J-Oras6uHjezRBS4ZbDt4K8hlhjA130_provenance.