Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_assertion> ?p ?o ?g. }
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- NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_assertion type Assertion NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_head.
- NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_assertion description "[Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_provenance.
- NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_assertion evidence source_evidence_literature NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_provenance.
- NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_assertion SIO_000772 19900826 NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_provenance.
- NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_assertion wasDerivedFrom befree-20140225 NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_provenance.
- NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_assertion wasGeneratedBy ECO_0000203 NP478748.RAQEYjqlMclF1hgaXVFeq3zrojk7gsEqHMDdvmfCkCsXs130_provenance.