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- NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_assertion type Assertion NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_head.
- NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_assertion description "[Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_provenance.
- NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_assertion evidence source_evidence_literature NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_provenance.
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- NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_assertion wasDerivedFrom befree-2016 NP592201.RAAiJrOwhaZ17QF6cJXMVD38Twd0-NxBbpCTB0Ztfpy1g130_provenance.
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