Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP585538.RAqbfowWdkLjrLk5SEIV6dR3kNlKXCU5MUwGemIXSquCI130_provenance.