Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion type Assertion NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_head.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_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." NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion evidence source_evidence_literature NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion SIO_000772 18499664 NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion wasDerivedFrom befree-20150227 NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.
- NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_assertion wasGeneratedBy ECO_0000203 NP871124.RAD0pbOW8ys8g1FE-439p2-exLDp1H82E-Ms1EPV0-3k4130_provenance.