Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_assertion evidence source_evidence_literature NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_assertion SIO_000772 17049295 NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_assertion wasDerivedFrom befree-20150227 NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_assertion wasGeneratedBy ECO_0000203 NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914811.RApnHe3c2drqwcXPOp4BvlJ1mvtSUXvmkdtb1YXqp0bCQ130_provenance.