Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP914453.RAv-6XvUGMAPkMf6fHnQh5ZsUcfDbP8_oW8mqPd36IjGQ130_provenance.