Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_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." NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_assertion evidence source_evidence_literature NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_assertion SIO_000772 15574464 NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_assertion wasDerivedFrom befree-20140225 NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_assertion wasGeneratedBy ECO_0000203 NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP475354.RA6Ig8AKaefGwVtUuuQ8mRUcKqSrMyIux4PivA_ZXpwOk130_provenance.