Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_assertion description "[Fragile X syndrome (FXS) mental retardation is caused by loss-of-function mutations in an RNA-binding protein, fragile X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_assertion evidence source_evidence_literature NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_assertion SIO_000772 18272470 NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_assertion wasDerivedFrom befree-20140225 NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_assertion wasGeneratedBy ECO_0000203 NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478441.RAHi_fgLYl7tzMwdou105krz5ITrlI6nvxYWEpBU28xTM130_provenance.