Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- befree-2016 importedOn "2016-02-19" NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_assertion wasGeneratedBy ECO_0000203 NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_assertion wasDerivedFrom befree-2016 NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_assertion SIO_000772 21212100 NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_assertion evidence source_evidence_literature NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.
- NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_assertion description "[Rett syndrome (RTT) is a neurodevelopmental disorder with no efficient treatment that is caused in the majority of cases by mutations in the gene methyl-CpG binding-protein 2 (MECP2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863582.RAKQCKtnpPmCA1p-8R2W5RHK7ctcFn4YWdoXU-LT3ZUds130_provenance.