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- NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_assertion type Assertion NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_head.
- NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_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." NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_provenance.
- NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_assertion evidence source_evidence_literature NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_provenance.
- NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_assertion SIO_000772 17273969 NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_provenance.
- NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_assertion wasDerivedFrom befree-20140225 NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_provenance.
- NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_assertion wasGeneratedBy ECO_0000203 NP573693.RAbgdoHLJrRbkCg7j6xYC6D4eAm_RCtjcL-g7dgXCj4D8130_provenance.