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- source_evidence_literature type ECO_0000212 NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_assertion description "[Spinocerebellar ataxia type 28 is an autosomal dominant form of cerebellar ataxia (ADCA) caused by mutations in AFG3L2, a gene that encodes a subunit of the mitochondrial m-AAA protease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_assertion evidence source_evidence_literature NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_assertion SIO_000772 20725928 NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_assertion wasDerivedFrom befree-20140225 NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_assertion wasGeneratedBy ECO_0000203 NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP295752.RA8pB7LgvQmPAe80usRSgAUQbI-YdN5lCK_PnORfKXvN8130_provenance.