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- NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_assertion type Assertion NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_head.
- NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_assertion wasGeneratedBy ECO_0000203 NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_provenance.
- NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_assertion wasDerivedFrom befree-20150227 NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_provenance.
- NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_assertion SIO_000772 15580558 NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_provenance.
- NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_assertion evidence source_evidence_literature NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_provenance.
- NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_assertion description "[We conclude that KCNJ11 mutations are a common cause of PNDM either in isolation or associated with developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522767.RAOCfug9AReJPMiznbl67ntxChV386wMDhJSRRhFv9mAM130_provenance.