Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_assertion description "[Premutation alleles of the fragile X mental retardation 1 (FMR1) gene give rise to a late-onset movement disorder, fragile X-associated tremor/ataxia syndrome (FXTAS), characterized by progressive intention tremor and gait ataxia, with associated dementia and global brain atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_assertion evidence source_evidence_literature NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_assertion SIO_000772 17133502 NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_assertion wasDerivedFrom befree-20140225 NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_assertion wasGeneratedBy ECO_0000203 NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP214629.RAC0Ppib11jghlB8xoGiY080EPEnOGBY8dBAWtvzBzRxU130_provenance.