Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion> ?p ?o ?g. }
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- NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion type Assertion NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_head.
- NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion wasGeneratedBy ECO_0000203 NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_provenance.
- NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion wasDerivedFrom befree-20140225 NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_provenance.
- NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion SIO_000772 19139306 NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_provenance.
- NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion evidence source_evidence_literature NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_provenance.
- NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509904.RA9uYxfkB3QcY4HyJ9AxeVy0MTH0cyY1IJFfXWG39WxIQ130_provenance.