Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_assertion> ?p ?o ?g. }
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- NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_assertion type Assertion NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_head.
- NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_assertion description "[We report a new point mutation in the p63 gene in a family in which the mother was initially diagnosed with Rapp-Hodgkin syndrome and her two offspring manifested ankyloblepharon, ectodermal defects, cleft lip and palate, syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_provenance.
- NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_assertion evidence source_evidence_literature NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_provenance.
- NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_assertion SIO_000772 16190990 NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_provenance.
- NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_assertion wasDerivedFrom befree-20150227 NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_provenance.
- NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_assertion wasGeneratedBy ECO_0000203 NP768052.RAqqpdx7nIiLLetdc6tE-Qmt9CCIcG94Iv7Tb4Su_e60A130_provenance.