Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_assertion> ?p ?o ?g. }
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- NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_assertion type Assertion NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_head.
- NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_assertion wasGeneratedBy ECO_0000203 NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_provenance.
- NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_assertion wasDerivedFrom befree-2016 NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_provenance.
- NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_assertion SIO_000772 21615690 NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_provenance.
- NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_assertion evidence source_evidence_literature NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_provenance.
- NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_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." NP897009.RAqeSicC3oxirc0w4Rk6ZgDITVSN0aXhgcI48jpyK0vys130_provenance.