Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_assertion> ?p ?o ?g. }
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- NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_assertion type Assertion NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_head.
- NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_assertion description "[This disease is one of the most common dominantly inherited ataxias worldwide; the defect in SCA3 is due to CAG repeat expansion (from the normal 14-41 to 55-82 repeats) in the ATXN3 coding region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_provenance.
- NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_assertion evidence source_evidence_literature NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_provenance.
- NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_assertion SIO_000772 25633985 NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_provenance.
- NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_assertion wasDerivedFrom befree-2016 NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_provenance.
- NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_assertion wasGeneratedBy ECO_0000203 NP1259436.RAUlC3iwCBn27w14Nxu6FP8cvdS7ewydViX9F9ZVs3S3E130_provenance.