Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_assertion description "[Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_assertion evidence source_evidence_literature NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_assertion SIO_000772 17098887 NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_assertion wasDerivedFrom befree-2016 NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_assertion wasGeneratedBy ECO_0000203 NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.
- befree-2016 importedOn "2016-02-19" NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_provenance.