Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_assertion> ?p ?o ?g. }
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- NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_assertion type Assertion NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_head.
- NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_assertion description "[Pathogenic mutations in episodic ataxia genes were excluded, thus making it highly unlikely that this phenotype was because of episodic ataxia as a second disorder besides LBSL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_provenance.
- NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_assertion evidence source_evidence_literature NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_provenance.
- NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_assertion SIO_000772 21749991 NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_provenance.
- NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_assertion wasDerivedFrom befree-20140225 NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_provenance.
- NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_assertion wasGeneratedBy ECO_0000203 NP939071.RAs0PLiUp6xIhIowKcAZ7CbnY9aBc0-gNJd8GolD5Cxoc130_provenance.