Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_assertion> ?p ?o ?g. }
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- NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_assertion type Assertion NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_head.
- NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_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." NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_provenance.
- NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_assertion evidence source_evidence_curated NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_provenance.
- NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_assertion SIO_000772 8872460 NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_provenance.
- NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_assertion wasDerivedFrom uniprot-2016 NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_provenance.
- NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_assertion wasGeneratedBy ECO_0000218 NP9186.RA6bfzkgQ2GmXaXvNLNbK-I-CrMe1ywLXaKVhdq2NsoHM130_provenance.