Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_assertion> ?p ?o ?g. }
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- NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_assertion type Assertion NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_head.
- NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_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." NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_provenance.
- NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_assertion evidence source_evidence_curated NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_provenance.
- NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_assertion SIO_000772 8872460 NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_provenance.
- NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_assertion wasDerivedFrom uniprot-20130724 NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_provenance.
- NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_assertion wasGeneratedBy ECO_0000218 NP1132.RAedXbbeyvriVl5Uw3Fa6LVesrGjnL84sjU1hKHjrR10E130_provenance.