Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_assertion> ?p ?o ?g. }
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- NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_assertion type Assertion NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_head.
- NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_assertion wasGeneratedBy ECO_0000203 NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_provenance.
- NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_assertion wasDerivedFrom befree-20140225 NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_provenance.
- NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_assertion SIO_000772 19139306 NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_provenance.
- NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_assertion evidence source_evidence_literature NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_provenance.
- NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_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." NP852142.RACzLIkIgvbtzhphAroezvvodQl2fiULR0phPAEzUNBMQ130_provenance.