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- NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_assertion type Assertion NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_head.
- NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_assertion description "[Three imprinted genes, MEST, MESTIT1, and COPG2IT1 on chromosome 7q32, are unlikely to cause SRS since epigenetic and sequence mutation analyses have not shown any changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_provenance.
- NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_assertion evidence source_evidence_literature NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_provenance.
- NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_assertion SIO_000772 12676894 NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_provenance.
- NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_assertion wasDerivedFrom befree-20140225 NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_provenance.
- NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_assertion wasGeneratedBy ECO_0000203 NP388549.RALCICs640uL0Cp-eJQ2bU8TZQjev7QMjaFUCN3Dkh-kg130_provenance.