Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_assertion> ?p ?o ?g. }
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- NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_assertion type Assertion NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_head.
- NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_assertion wasGeneratedBy ECO_0000203 NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_provenance.
- NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_assertion wasDerivedFrom befree-20150227 NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_provenance.
- NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_assertion SIO_000772 19239083 NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_provenance.
- NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_assertion evidence source_evidence_literature NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_provenance.
- NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_assertion description "[The ankyloblepharon-ectodermal defects-cleft lip and palate (Hay-Wells or AEC) and the Rapp-Hodgkin syndrome (RHS) are rare autosomal dominant ectodermal dysplasias due to mutations in the transcription factor gene P63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857166.RA8Mzxu8BJwlRUnoPv-_o-jTmjRMV-jxmgHwI78qoNsQs130_provenance.