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- NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_assertion type Assertion NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_head.
- NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_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." NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_provenance.
- NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_assertion evidence source_evidence_literature NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_provenance.
- NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_assertion SIO_000772 17273969 NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_provenance.
- NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_assertion wasDerivedFrom befree-20140225 NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_provenance.
- NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_assertion wasGeneratedBy ECO_0000203 NP790031.RAIi2Pe817Tx_WbHSzPnIvqs-La8QdWnLPqPGjiCPwEqA130_provenance.