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- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion type Assertion NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_head.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion description "[FHL1 mutations cause Emery-Dreifuss muscular dystrophy (OMIM 310300), X-linked myopathy with postural muscle atrophy (XMPMA, OMIM 300696), scapuloperoneal myopathy (OMIM 300695), or reducing body myopathy (OMIM 300717, 300718).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion evidence source_evidence_literature NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion SIO_000772 21932316 NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion wasDerivedFrom befree-20150227 NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion wasGeneratedBy ECO_0000203 NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.