Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_assertion description "[Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_assertion evidence source_evidence_literature NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_assertion SIO_000772 23332917 NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_assertion wasDerivedFrom befree-20150227 NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_assertion wasGeneratedBy ECO_0000203 NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932981.RA9tlkh6Qn6xUjwKFX1m7hsa9S8SCDX9U1gvQ-dFJSdeU130_provenance.