Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_assertion> ?p ?o ?g. }
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- NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_assertion type Assertion NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_head.
- NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_assertion wasGeneratedBy ECO_0000203 NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_provenance.
- NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_assertion wasDerivedFrom befree-20150227 NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_provenance.
- NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_assertion SIO_000772 18499664 NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_provenance.
- NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_assertion evidence source_evidence_literature NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_provenance.
- NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_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." NP989222.RADCUIo7pUc4yUB7zPb-PnQt8-PyEXaU-GOcDq37QCTOk130_provenance.