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- NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_assertion type Assertion NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_head.
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- NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_assertion wasDerivedFrom befree-20150227 NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_provenance.
- NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_assertion SIO_000772 22344793 NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_provenance.
- NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_assertion evidence source_evidence_literature NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_provenance.
- NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_assertion description "[Association of X-linked hydrocephalus and Hirschsprung disease: report of a new patient with a mutation in the L1CAM gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768348.RANLd09F5jMI2VnIG96CKavE7YJ4X7xaTe-FfEz0tkT84130_provenance.