Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_assertion> ?p ?o ?g. }
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- NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_assertion type Assertion NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_head.
- NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_assertion wasGeneratedBy ECO_0000203 NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_provenance.
- NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_assertion wasDerivedFrom befree-2016 NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_provenance.
- NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_assertion SIO_000772 23297359 NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_provenance.
- NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_assertion evidence source_evidence_literature NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_provenance.
- NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_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." NP1041599.RAtBOjqiHbZI6LlpjQ7ZMvf1Om15pz8OLged5hIOXIXuY130_provenance.