Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_assertion description "[Elimination of the native structure and solubility of the hVAPB MSP domain by the Pro56Ser mutation that causes amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_assertion evidence source_evidence_literature NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_assertion SIO_000772 20377183 NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_assertion wasDerivedFrom befree-20150227 NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_assertion wasGeneratedBy ECO_0000203 NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP570864.RAJFj_fmtW9t2XGQ5K9iyngRMWFG4aOqLsDQQfaf9D63Y130_provenance.