Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- befree-2016 importedOn "2016-02-19" NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_assertion wasGeneratedBy ECO_0000203 NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_assertion wasDerivedFrom befree-2016 NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_assertion SIO_000772 20430935 NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_assertion evidence source_evidence_literature NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.
- NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_assertion description "[The clinical features of FXTAS, as well as other forms of clinical involvement in carriers without FXTAS, are thought to arise from a toxic gain of function of transcriptionally active FMR1 containing expanded CGG repeats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809310.RAO5MEwUaidyGOuvrkwUfwieV-8C_TJ0Qax7uZvTMKmwU130_provenance.