Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_assertion> ?p ?o ?g. }
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- NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_assertion type Assertion NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_head.
- NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_assertion description "[Mutations in the Senataxin gene (SETX) are associated with autosomal recessive ataxia-ocular apraxia 2 (AOA2) and autosomal dominant juvenile ALS (ALS4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_provenance.
- NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_assertion evidence source_evidence_literature NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_provenance.
- NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_assertion SIO_000772 16717225 NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_provenance.
- NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_assertion wasDerivedFrom befree-20150227 NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_provenance.
- NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_assertion wasGeneratedBy ECO_0000203 NP867851.RA4HYGZrmkG4B3l9BHICc8EbbXRx1mbyVrHbFesWICycE130_provenance.