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- NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_assertion type Assertion NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_head.
- NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_assertion wasGeneratedBy ECO_0000203 NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_provenance.
- NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_assertion wasDerivedFrom befree-20150227 NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_provenance.
- NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_assertion SIO_000772 7840347 NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_provenance.
- NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_assertion evidence source_evidence_literature NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_provenance.
- NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_assertion description "[Over the past 3 years, reports of DNA alteration in myotonic dystrophy, fragile X syndrome (types A and E), Kennedy's disease, Huntington's disease, spinocerebellar ataxia type 1, and dentatorubral-pallidoluysian atrophy have identified a new class of human mutation, referred to as trinucleotide repeat amplification.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP896826.RAOiDVS-GZjvDCSe9dlLptzfIumKQEvi2vud6LY81y6H8130_provenance.