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- NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_assertion type Assertion NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_head.
- NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_assertion description "[Epigenetic allele silencing unveils recessive RYR1 mutations in core myopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_provenance.
- NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_assertion evidence source_evidence_literature NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_provenance.
- NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_assertion SIO_000772 17033962 NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_provenance.
- NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_assertion wasDerivedFrom befree-2016 NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_provenance.
- NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_assertion wasGeneratedBy ECO_0000203 NP573793.RAdam1H21X3cd60SOoC9J_TFWRc4GopYxEui43hbrMlfo130_provenance.