Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion> ?p ?o ?g. }
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- NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion type Assertion NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_head.
- NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion description "[New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_provenance.
- NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion evidence source_evidence_curated NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_provenance.
- NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion SIO_000772 8872460 NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_provenance.
- NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion wasDerivedFrom uniprot-20130724 NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_provenance.
- NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_assertion wasGeneratedBy ECO_0000218 NP1136.RAqqW3vjMFtgcw-C5ffQCrDrm1s1psuYJi6qDQT8YXEr4130_provenance.