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- NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_assertion type Assertion NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_head.
- NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_assertion wasGeneratedBy ECO_0000203 NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_provenance.
- NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_assertion wasDerivedFrom befree-2016 NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_provenance.
- NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_assertion SIO_000772 21615690 NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_provenance.
- NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_assertion evidence source_evidence_literature NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_provenance.
- NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_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." NP897011.RA0ns137GuLEw5_h47kZc8jzE1nca2rkRuEgw0SiA2nUk130_provenance.