Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion> ?p ?o ?g. }
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- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion type Assertion NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_head.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion description "[Myotonic dystrophy (DM), the most common inherited muscle disorder, is caused by a CTG expansion in the 3`-untranslated region of a protein kinase gene ( DMPK ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion evidence source_evidence_literature NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion SIO_000772 10332033 NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion wasDerivedFrom befree-20140225 NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.
- NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_assertion wasGeneratedBy ECO_0000203 NP250133.RAWet5GsZsj9_EQRdj_6K7dpcJFLrPhnGffUE_ZEiWXQA130_provenance.