Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_assertion> ?p ?o ?g. }
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- NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_assertion type Assertion NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_head.
- NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_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." NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_provenance.
- NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_assertion evidence source_evidence_literature NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_provenance.
- NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_assertion SIO_000772 16190990 NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_provenance.
- NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_assertion wasDerivedFrom befree-20150227 NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_provenance.
- NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_assertion wasGeneratedBy ECO_0000203 NP675003.RALmy1JxDqOGmc0gWCBLwVdDjaeysHbvLfl3qOvCqV_6E130_provenance.