Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion> ?p ?o ?g. }
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- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion type Assertion NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_head.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion wasGeneratedBy ECO_0000203 NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion wasDerivedFrom befree-20150227 NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion SIO_000772 19139306 NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_assertion evidence source_evidence_literature NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.
- NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_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." NP695409.RAhH5tnsCJLkRKQc1zQYB78Yiy1o24UVzIl0Kfba8HSoI130_provenance.