Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_assertion> ?p ?o ?g. }
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- NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_assertion type Assertion NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_head.
- NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_assertion description "[The mutation causing myotonic dystrophy (DM) has recently been identified as an unstable CTG trinucleotide repeat located in the 3' untranslated region of a gene encoding for a protein with putative serine-threonine protein kinase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_provenance.
- NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_assertion evidence source_evidence_literature NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_provenance.
- NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_assertion SIO_000772 8499920 NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_provenance.
- NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_assertion wasDerivedFrom befree-20140225 NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_provenance.
- NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_assertion wasGeneratedBy ECO_0000203 NP291502.RAlsCEqdIo-77jNAERDxgP9bAQ_lkD6c56tP80iJ15J0I130_provenance.