Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_assertion description "[Our study shows that spastin mutations are a frequent cause of apparently sporadic spastic paraparesis but not of primary lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_assertion evidence source_evidence_literature NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_assertion SIO_000772 16240363 NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_assertion wasDerivedFrom befree-2016 NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_assertion wasGeneratedBy ECO_0000203 NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.
- befree-2016 importedOn "2016-02-19" NP518979.RAuUDYXxOoGYfeo8_s0b4wYQixUqzFcVTTTFhfmdjTFxw130_provenance.