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- NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_assertion type Assertion NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_head.
- NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_assertion description "[The SMADIP1 gene recently has been recognized as disease causing in some patients with 2q22 chromosomal rearrangement, resulting in syndromic HSCR with mental retardation, with microcephaly, and with facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_provenance.
- NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_assertion evidence source_evidence_literature NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_provenance.
- NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_assertion SIO_000772 11595972 NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_provenance.
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- NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_assertion wasGeneratedBy ECO_0000203 NP420585.RAfZ-YoD6J59KqF_vH-n0A-E-FgQ-OQROwrp3-FTQ8JMc130_provenance.