Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_assertion> ?p ?o ?g. }
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- NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_assertion type Assertion NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_head.
- NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_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." NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_provenance.
- NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_assertion evidence source_evidence_literature NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_provenance.
- NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_assertion SIO_000772 18807109 NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_provenance.
- NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_assertion wasDerivedFrom befree-2016 NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_provenance.
- NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_assertion wasGeneratedBy ECO_0000203 NP694331.RAH6jNQ9oCIVy-VmLXK-8Dvg6ON8D95BGHwF3kaqoZUWM130_provenance.