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- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion type Assertion NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_head.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion evidence source_evidence_literature NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion SIO_000772 17273969 NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion wasDerivedFrom befree-20140225 NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion wasGeneratedBy ECO_0000203 NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.