Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP911169.RAulT-z3hH6f7vWeOp4rm9AjcUtn3ZRlvXZd0-tN9ra8w130_provenance.