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- source_evidence_literature type ECO_0000212 NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_assertion wasGeneratedBy ECO_0000203 NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_assertion wasDerivedFrom befree-20140225 NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_assertion SIO_000772 23297359 NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_assertion evidence source_evidence_literature NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_assertion description "[Mutations in CLN6 were recently identified in recessive Kufs disease presenting as progressive myoclonus epilepsy (Type A), whereas the molecular basis of cases presenting with dementia and motor features (Type B) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682487.RAIoK4oeY_WkHh80MJHs0mXNv57VoTKX8lNZuJ9gJxZNI130_provenance.