Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_assertion> ?p ?o ?g. }
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- NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_assertion type Assertion NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_head.
- NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_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." NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.
- NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_assertion evidence source_evidence_literature NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.
- NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_assertion SIO_000772 16717225 NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.
- NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_assertion wasDerivedFrom befree-20140225 NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.
- NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_assertion wasGeneratedBy ECO_0000203 NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.