Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_assertion description "[Another novel spastin mutation was found in a patient with a rapidly progressive spinal and bulbar UMN syndrome that progressed to amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_assertion evidence source_evidence_literature NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_assertion SIO_000772 16240363 NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_assertion wasDerivedFrom befree-2016 NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_assertion wasGeneratedBy ECO_0000203 NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.
- befree-2016 importedOn "2016-02-19" NP518980.RAFnKdUh8QuKJTubIjDsbRT2JzW6JnBVqcQOGq5x1kYYs130_provenance.