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- NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_assertion type Assertion NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_head.
- NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_assertion wasGeneratedBy ECO_0000203 NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_provenance.
- NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_assertion wasDerivedFrom befree-20140225 NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_provenance.
- NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_assertion SIO_000772 10597140 NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_provenance.
- NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_assertion evidence source_evidence_literature NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_provenance.
- NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_assertion description "[Epidermolytic hyperkeratosis (EHK) is a genodermatosis caused by mutations in either the keratin 1 (K1) or keratin 10 (K10) genes, and characterized by erythroderma and blistering at birth, with development of a ribbed, ichthyotic hyperkeratosis and palmoplantar keratoderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887926.RAPsrurakUR0YRBwY9wD8-6aJcXg15ifLI0U9abbDfdok130_provenance.