Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion> ?p ?o ?g. }
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- NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion type Assertion NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_head.
- NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion description "[SETX mutations are a frequent genetic cause of juvenile and adult onset cerebellar ataxia with neuropathy and elevated serum alpha-fetoprotein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_provenance.
- NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion evidence source_evidence_literature NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_provenance.
- NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion SIO_000772 23941260 NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_provenance.
- NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion wasDerivedFrom befree-2016 NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_provenance.
- NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_assertion wasGeneratedBy ECO_0000203 NP1102135.RAXZwDteX5UMTjqcPHWKYhHJkj9IZnHkoRpOpqNejTUXc130_provenance.