Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_assertion> ?p ?o ?g. }
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- NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_assertion type Assertion NP578850.RArqTjl2aFUQ3ZuqJjkOhKZCdGGvkageJHXxvJGmbkRYE130_head.
- 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.