Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion> ?p ?o ?g. }
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- NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion type Assertion NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_head.
- NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion description "[Except the PMP22 duplication, disease causing CNVs are rare but may cause CMT in about 1% (95% CI 0-7%) of the Norwegian CMT families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_provenance.
- NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion evidence source_evidence_literature NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_provenance.
- NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion SIO_000772 25648254 NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_provenance.
- NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion wasDerivedFrom befree-2016 NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_provenance.
- NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_assertion wasGeneratedBy ECO_0000203 NP1260755.RAamO9VGReMiwcfDBZs9dRqasZe2JEz19ZluMQWFLltxs130_provenance.