Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_assertion> ?p ?o ?g. }
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- NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_assertion type Assertion NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_head.
- NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_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." NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_provenance.
- NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_assertion evidence source_evidence_curated NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_provenance.
- NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_assertion SIO_000772 8872460 NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_provenance.
- NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_assertion wasDerivedFrom uniprot-20130724 NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_provenance.
- NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_assertion wasGeneratedBy ECO_0000218 NP1121.RA7rWVlj12f4NJ4Ewq6JAgUmSP_WkvEzoCxEPhrtqC4eg130_provenance.