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- source_evidence_literature type ECO_0000212 NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_assertion description "[Consistent with a function of Rab11 in Schwann cell myelination, SH3TC2 mutations that cause neuropathy disrupt the SH3TC2/Rab11 interaction, and forced expression of dominant negative Rab11 strongly impairs myelin formation in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_assertion evidence source_evidence_literature NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_assertion SIO_000772 20826437 NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_assertion wasDerivedFrom befree-2016 NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_assertion wasGeneratedBy ECO_0000203 NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.
- befree-2016 importedOn "2016-02-19" NP838025.RAlxAbe4HYBuoZT3b3v2JTiBSkQLEACkBkaZi-2qupeTM130_provenance.