Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_assertion> ?p ?o ?g. }
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- NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_assertion type Assertion NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_head.
- NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_assertion description "[Today more than 30 different mutations in this gene have been defined and associated with PMD or the clinically distinct form X-linked spastic paraplegia type-2 (SPG-2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_provenance.
- NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_assertion evidence source_evidence_literature NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_provenance.
- NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_assertion SIO_000772 8520726 NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_provenance.
- NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_assertion wasDerivedFrom befree-20140225 NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_provenance.
- NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_assertion wasGeneratedBy ECO_0000203 NP237787.RAZVZejNJPZOCRg6PWX_fZE1k54O-0tBf5Bq0-sU17rS0130_provenance.