Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_assertion> ?p ?o ?g. }
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- NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_assertion type Assertion NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_head.
- NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_assertion description "[Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_provenance.
- NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_assertion evidence source_evidence_curated NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_provenance.
- NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_assertion SIO_000772 25192047 NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_provenance.
- NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_assertion wasDerivedFrom uniprot-2016 NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_provenance.
- NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_assertion wasGeneratedBy ECO_0000218 NP8006.RAb6cNcDdugQHVA4kVWzrirjagcT8kPRoDitjpOIA8kp0130_provenance.