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- NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_assertion type Assertion NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_head.
- NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_assertion wasGeneratedBy ECO_0000203 NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_provenance.
- NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_assertion wasDerivedFrom befree-20140225 NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_provenance.
- NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_assertion SIO_000772 9268105 NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_provenance.
- NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_assertion evidence source_evidence_literature NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_provenance.
- NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_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." NP931441.RA9qG8C2MyE2Sjb0h1M8e_7H86JfVY7SmmaRgSi8IQyC8130_provenance.