Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion type Assertion NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_head.
- NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion description "[Myotonic dystrophy type 2/proximal myotonic myopathy (DM2/PROMM) is an autosomal dominant multisystem disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_provenance.
- NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion evidence source_evidence_literature NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_provenance.
- NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion SIO_000772 15596616 NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_provenance.
- NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion wasDerivedFrom befree-2016 NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_provenance.
- NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_assertion wasGeneratedBy ECO_0000203 NP472591.RAIIefKBx97Zg9fQUC3af9pZ86YmRcV_yxgPU2MZOWhU8130_provenance.