Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_assertion> ?p ?o ?g. }
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- NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_assertion type Assertion NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_head.
- NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_assertion wasGeneratedBy ECO_0000203 NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_provenance.
- NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_assertion wasDerivedFrom befree-2016 NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_provenance.
- NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_assertion SIO_000772 18499664 NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_provenance.
- NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_assertion evidence source_evidence_literature NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_provenance.
- NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_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." NP672829.RA-uW0DL8ELnsy0OKRR8aJ8vYPZD1JyUUKKK1Gd6f70cw130_provenance.