Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_assertion description "[Expansion of a polymorphic GCC-repeat at the FRAXE locus has been associated with expression of chromosome fragility at this site and cognitive impairment in some individuals previously testing negative for CGG-repeat expansion in the fragile X mental retardation-1 (FMR1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_assertion evidence source_evidence_literature NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_assertion SIO_000772 8844096 NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_assertion wasDerivedFrom befree-20140225 NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_assertion wasGeneratedBy ECO_0000203 NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP182290.RA5PAevfg2MVVCX3nOJFjLfQ9vMxclfFBIqCX0iMnkhpk130_provenance.