Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_assertion description "[Interestingly, all three analyzed myotilin missense mutations (S55F, S60F and S60C) do not lead to gross changes in the total amount of myotilin or to aberrant posttranslational modifications in diseased muscle, as observed in a number of muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_assertion evidence source_evidence_literature NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_assertion SIO_000772 16684602 NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_assertion wasDerivedFrom befree-20150227 NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_assertion wasGeneratedBy ECO_0000203 NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP824729.RAjUERorABVWM6gyH7XwMbnRlAzSl_g8Gi7xntm3Am8lY130_provenance.