Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion type Assertion NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_head.
- NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion description "[These data provide the first evidence that the ER-retention of mutant FKRP may play a role in the pathogenesis of CMD and potentially explain why the allelic disorder LGMD2I is milder, because the mutated protein is able to reach the Golgi apparatus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_provenance.
- NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion evidence source_evidence_literature NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_provenance.
- NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion SIO_000772 15574464 NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_provenance.
- NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion wasDerivedFrom befree-2016 NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_provenance.
- NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_assertion wasGeneratedBy ECO_0000203 NP470863.RA_GGNo9acs2Hgbd9zX2mJ40jTiXG4WLjemmnxySz0dss130_provenance.