Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_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." NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_assertion evidence source_evidence_literature NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_assertion SIO_000772 20826437 NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_assertion wasDerivedFrom befree-20150227 NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_assertion wasGeneratedBy ECO_0000203 NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP944622.RAs8qmjM4Kq54MkN-tG0XztH-MPigkCoJmKU1J1edLaTA130_provenance.