Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_assertion type Assertion NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_head.
- NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_assertion wasGeneratedBy ECO_0000203 NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_provenance.
- NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_assertion wasDerivedFrom befree-20150227 NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_provenance.
- NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_assertion SIO_000772 21615690 NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_provenance.
- NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_assertion evidence source_evidence_literature NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_provenance.
- NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_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." NP857169.RAvBgOcBIN6kDgeqmKXLNk0VF7mRqcOuIvjAg8pHKKYOo130_provenance.