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- NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_assertion type Assertion NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_head.
- NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_assertion wasGeneratedBy ECO_0000203 NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_provenance.
- NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_assertion wasDerivedFrom befree-2016 NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_provenance.
- NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_assertion SIO_000772 16237566 NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_provenance.
- NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_assertion evidence source_evidence_literature NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_provenance.
- NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_assertion description "[For SMARCAL1 mutations a clear genotype-phenotype correlation has been reported: severe SIOD with in utero or early-childhood onset leading to end-stage renal disease within a few years is caused by nonsense, frame shift or splice mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518754.RAHijTxvsWmO-2-I11Ky_Eh1LoRV39bqK8Ighde8vVjFc130_provenance.