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- NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_assertion type Assertion NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_head.
- NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_assertion wasGeneratedBy ECO_0000203 NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_provenance.
- NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_assertion wasDerivedFrom befree-20140225 NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_provenance.
- NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_assertion SIO_000772 11739371 NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_provenance.
- NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_assertion evidence source_evidence_literature NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_provenance.
- NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_assertion description "[Lafora disease (progressive myoclonus epilepsy of Lafora type) is an autosomal recessive neurodegenerative disorder resulting from defects in the EPM2A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP546306.RAJ9VYO5Hqp0ARsWlEYWFm2fkW5vkojc4o4gkMlCNLMKk130_provenance.