Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_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." NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_assertion evidence source_evidence_literature NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_assertion SIO_000772 20826437 NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_assertion wasDerivedFrom befree-20140225 NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_assertion wasGeneratedBy ECO_0000203 NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212329.RAb_zGVbi0fTooWfGDpuSN-0cxjvAL9UhEPxQrH-F_oyw130_provenance.