Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion type Assertion NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_head.
- NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion description "[The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_provenance.
- NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion evidence source_evidence_literature NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_provenance.
- NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion SIO_000772 8162055 NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_provenance.
- NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion wasDerivedFrom befree-20150227 NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_provenance.
- NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_assertion wasGeneratedBy ECO_0000203 NP409242.RA3Javw02wzfOm3tQ2Rh_cMC_bPHGOC5c87XGzhNI0c54130_provenance.