Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP600768.RA5Dt4QDbMaU0e3dOF4WZIEFuvA-CUfWaCv__YPkUsZIY130_provenance.