Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_assertion> ?p ?o ?g. }
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- NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_assertion type Assertion NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_head.
- NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_assertion description "[The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_provenance.
- NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_assertion evidence source_evidence_literature NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_provenance.
- NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_assertion SIO_000772 24369382 NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_provenance.
- NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_assertion wasDerivedFrom befree-20150227 NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_provenance.
- NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_assertion wasGeneratedBy ECO_0000203 NP907952.RAQbQjvgxkozTZYQelNJ1WutLB-ehn99s_hcyeXjVh7QI130_provenance.