Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion type Assertion NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_head.
- NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion description "[Mutations in RYR1 are associated with several congenital myopathies (termed RYR1-related myopathies) that are the most common non-dystrophic muscle diseases of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_provenance.
- NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion evidence source_evidence_literature NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_provenance.
- NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion SIO_000772 22418739 NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_provenance.
- NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion wasDerivedFrom befree-20140225 NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_provenance.
- NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_assertion wasGeneratedBy ECO_0000203 NP507265.RAGbhlkp6iDMu3Lq_OPMkW0Bij7B5tWZLJpgEOkBpdHNs130_provenance.