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- NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_assertion type Assertion NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_head.
- NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_assertion description "[Myotonic dystrophy type 1 (DM1) is a neuromuscular disease caused by the expansion of a CTG repeat in the DMPK gene and characterised by progressive skeletal muscle weakness and wasting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_provenance.
- NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_assertion evidence source_evidence_literature NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_provenance.
- NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_assertion SIO_000772 20346670 NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_provenance.
- NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_assertion wasDerivedFrom befree-20150227 NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_provenance.
- NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_assertion wasGeneratedBy ECO_0000203 NP355958.RAW_bW-sRcyn2YVvnZfjHIe10l9F9W9PTjgVcdhu6e5QI130_provenance.