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- NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_assertion type Assertion NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_head.
- NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_assertion description "[Netherton syndrome (NS) is a severe genetic skin disease in which absence of a key protease inhibitor causes congenital exfoliative erythroderma, eczematous-like lesions, and atopic manifestations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_provenance.
- NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_assertion evidence source_evidence_literature NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_provenance.
- NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_assertion SIO_000772 24534191 NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_provenance.
- NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_assertion wasDerivedFrom befree-20150227 NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_provenance.
- NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_assertion wasGeneratedBy ECO_0000203 NP989563.RAm_n7QhwH9EyuKQe4pXfBD1L_1uqYXF9UNNbdxa0dBLs130_provenance.