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- source_evidence_literature type ECO_0000212 NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_assertion description "[This produced an early-onset clinical syndrome that combines the severe phenotypes of SPG7 and SCA28, in additional to other mitochondrial features such as oculomotor apraxia, extrapyramidal dysfunction, and myoclonic epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_assertion evidence source_evidence_literature NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_assertion SIO_000772 22022284 NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_assertion wasDerivedFrom befree-2016 NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_assertion wasGeneratedBy ECO_0000203 NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.
- befree-2016 importedOn "2016-02-19" NP933158.RAS8tpE-sC8BlqW6TMn56hnl1wRya4ZXjHl0j-NDdhA1M130_provenance.