Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion type Assertion NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_head.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion description "[High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion evidence source_evidence_literature NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion SIO_000772 18807109 NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion wasDerivedFrom befree-2016 NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.
- NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_assertion wasGeneratedBy ECO_0000203 NP694330.RAgg3KiDG0RxFCOGZiEaqYbRBB4tp_ZUInEs6mNGBv2oU130_provenance.