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- NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_assertion type Assertion NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_head.
- NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_assertion wasGeneratedBy ECO_0000203 NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.
- NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_assertion wasDerivedFrom befree-20140225 NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.
- NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_assertion SIO_000772 23335487 NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.
- NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_assertion evidence source_evidence_literature NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.
- NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_assertion description "[Our data reveal a broad range of epimutations exist in certain imprinting syndromes, with the exception of Prader-Willi syndrome and Angelman syndrome patients that are associated with solitary SNRPN-DMR defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.