Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_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." NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_assertion evidence source_evidence_literature NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_assertion SIO_000772 16684602 NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_assertion wasDerivedFrom befree-2016 NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_assertion wasGeneratedBy ECO_0000203 NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.
- befree-2016 importedOn "2016-02-19" NP548829.RAd-u1FkU9RZahNrkVsVVlSCfUV6a87D4x2BRqX00Kz-0130_provenance.