Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_assertion> ?p ?o ?g. }
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- NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_assertion type Assertion NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_head.
- NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_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." NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_provenance.
- NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_assertion evidence source_evidence_literature NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_provenance.
- NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_assertion SIO_000772 15574464 NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_provenance.
- NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_assertion wasDerivedFrom befree-20140225 NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_provenance.
- NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_assertion wasGeneratedBy ECO_0000203 NP651959.RAIB7luV6K1pqt8kzAPm9ZqUc-gkCNWiD5tEgAVhcE3lw130_provenance.