Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_assertion> ?p ?o ?g. }
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- NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_assertion type Assertion NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_head.
- NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_assertion description "[Interestingly, in the largest SAX2 family, the presenting clinical sign was dysarthria, which is not common in other forms of inherited ataxias or spastic ataxias, whereas gait difficulties appeared later.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_provenance.
- NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_assertion evidence source_evidence_literature NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_provenance.
- NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_assertion SIO_000772 17273843 NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_provenance.
- NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_assertion wasDerivedFrom befree-2016 NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_provenance.
- NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_assertion wasGeneratedBy ECO_0000203 NP592039.RAaISMQF9EG95zMSuK2QZ4XYkQ4iNa4STZrT24FyV4edM130_provenance.