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- NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_assertion type Assertion NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_head.
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- NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_assertion SIO_000772 23018678 NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_provenance.
- NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_assertion evidence source_evidence_literature NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_provenance.
- NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_assertion description "[Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1016151.RAx6dKzfYU2QyUNosTESI0m2lJtmTaa_HOvzud2FpWXFw130_provenance.