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- source_evidence_literature type ECO_0000212 NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_assertion description "[Using clinical exome sequencing, we have detected three novel de novo SCN8A mutations in patients with intellectual disabilities, and variable clinical features including seizures in two patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_assertion evidence source_evidence_literature NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_assertion SIO_000772 25725044 NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_assertion wasDerivedFrom befree-2016 NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_assertion wasGeneratedBy ECO_0000203 NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.
- befree-2016 importedOn "2016-02-19" NP1266968.RABtnEnB7kM59tPslBM1llj6tqad-0JKFVpbOa3u377ws130_provenance.