Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_assertion description "[A mutant lacking this sequence can increase the nuclear distribution of IBMPFD VCP, suggesting that this sequence is a potential molecular target for correcting the deficient nucleocytoplasmic shuttling of IBMPFD VCP proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_assertion evidence source_evidence_literature NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_assertion SIO_000772 25447673 NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_assertion wasDerivedFrom befree-20150227 NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_assertion wasGeneratedBy ECO_0000203 NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768952.RAZy-tjt_0Cafk9xsqDT-_UiBPOmO7AWY9QpCfVUbleZA130_provenance.