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- NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_assertion type Assertion NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_head.
- NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_assertion wasGeneratedBy ECO_0000203 NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_provenance.
- NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_assertion wasDerivedFrom befree-20150227 NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_provenance.
- NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_assertion SIO_000772 9268105 NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_provenance.
- NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_assertion evidence source_evidence_literature NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_provenance.
- NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_assertion description "[Interestingly, a missense mutation in an XHC family predicting the Val768Ile change in the second fibronectin type III domain of L1CAM was found not only in the two affected cousins and their obligate carrier mothers but also in two unaffected male relatives of the patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409916.RAn3fzmWepQH1QlFfWXm6KCNh6K1iU5vjopwHMzMRt8GE130_provenance.