Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_assertion> ?p ?o ?g. }
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- NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_assertion type Assertion NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_head.
- NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_assertion description "[Fragile X-associated tremor/ataxia syndrome is a late adult onset neurodegenerative disorder that affects individuals who carry a premutation CGG repeat expansion (55-200 CGG repeats) in the 5' untranslated portion of the fragile X mental retardation 1 (FMR1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_provenance.
- NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_assertion evidence source_evidence_literature NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_provenance.
- NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_assertion SIO_000772 19794313 NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_provenance.
- NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_assertion wasDerivedFrom befree-2016 NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_provenance.
- NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_assertion wasGeneratedBy ECO_0000203 NP766572.RAWghSfxlygEjJKC-PbjeKPTKRaE6ls1_NO4_ngiJkp_0130_provenance.