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- NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_assertion type Assertion NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_head.
- NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_assertion wasGeneratedBy ECO_0000203 NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_provenance.
- NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_assertion wasDerivedFrom befree-20140225 NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_provenance.
- NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_assertion SIO_000772 18499664 NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_provenance.
- NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_assertion evidence source_evidence_literature NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_provenance.
- NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_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." NP523629.RAhJ9zYmMOcW5vO0d3K_B9ZXsIbolw1XnMI3Sk_D-fFAE130_provenance.