Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_assertion type Assertion NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_head.
- NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_assertion description "[Mutations of the MECP2 (methyl-CpG-binding protein) gene mainly cause Rett syndrome but were also shown to be involved in mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.
- NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_assertion evidence source_evidence_literature NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.
- NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_assertion SIO_000772 17383248 NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.
- NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_assertion wasDerivedFrom befree-2016 NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.
- NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_assertion wasGeneratedBy ECO_0000203 NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.