Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion> ?p ?o ?g. }
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- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion type Assertion NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_head.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion description "[Among the 15 sporadic SCA patients, genetic mutations for SCA2, SCA6, SCA17, and SCA31 were identified, indicating that ADCAs should be considered in sporadic cases of ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion evidence source_evidence_literature NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion SIO_000772 21088341 NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion wasDerivedFrom befree-2016 NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.
- NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_assertion wasGeneratedBy ECO_0000203 NP853351.RAjKT6JUwNKmYfhDT5B8anIc2ARTih_nmNNZIHVhSBVQA130_provenance.