Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_assertion> ?p ?o ?g. }
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- NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_assertion type Assertion NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_head.
- NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_assertion description "[In the majority of cases HNPP is caused by deletion of the peripheral myelin protein 22 gene (PMP22) on chromosome 17p11.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.
- NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_assertion evidence source_evidence_literature NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.
- NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_assertion SIO_000772 17183456 NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.
- NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_assertion wasDerivedFrom befree-2016 NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.
- NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_assertion wasGeneratedBy ECO_0000203 NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.