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- NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_assertion type Assertion NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_head.
- NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_assertion description "[Suggested as a candidate gene for a dominant syndrome that consists of inclusion body myopathy, Paget disease of bone, and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_provenance.
- NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_assertion evidence source_evidence_literature NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_provenance.
- NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_assertion SIO_000772 11749051 NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_provenance.
- NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_assertion wasDerivedFrom lhgdn-20090331 NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_provenance.
- NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_assertion wasGeneratedBy ECO_0000203 NP192738.RAgkop_citnvE5ioLMZu-PZH_PqepKPv7naMYffL1lNeM130_provenance.