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- NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_assertion type Assertion NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_head.
- NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_assertion wasGeneratedBy ECO_0000203 NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_provenance.
- NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_assertion wasDerivedFrom befree-2016 NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_provenance.
- NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_assertion SIO_000772 18499664 NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_provenance.
- NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_assertion evidence source_evidence_literature NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_provenance.
- NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_assertion description "[Most cases of Rett syndrome (RTT) are caused by mutations in the methylated DNA-binding protein, MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP672827.RAI5CSe7WmzzGaH2319SRLSOSsWjgnX-aPrQfHtpgzT9U130_provenance.