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- NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_assertion type Assertion NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_head.
- NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_assertion description "[We propose that familial cortical myoclonus is a novel movement disorder that may be caused by mutation in NOL3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_provenance.
- NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_assertion evidence source_evidence_literature NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_provenance.
- NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_assertion SIO_000772 22926851 NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_provenance.
- NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_assertion wasDerivedFrom befree-2016 NP1008463.RAgXamw-xxnz2p7U94R4Ym7DGFkM7rjrzpPy6KdNPBTwI130_provenance.
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