Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion> ?p ?o ?g. }
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- NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion type Assertion NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_head.
- NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion wasGeneratedBy ECO_0000203 NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_provenance.
- NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion wasDerivedFrom befree-20150227 NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_provenance.
- NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion SIO_000772 23297359 NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_provenance.
- NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion evidence source_evidence_literature NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_provenance.
- NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915736.RAXBalm9uvrRcFOw0pM61REEocKdiBDN3zHo0M9plcGBo130_provenance.