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- NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_assertion type Assertion NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_head.
- NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_assertion description "[Rare variants in these 5 genes likely or possibly caused 10.6% of DCM in this cohort. When combined with our prior resequencing reports, approximately 27% of DCM probands had possible or likely disease-causing variants identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_provenance.
- NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_assertion evidence source_evidence_literature NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_provenance.
- NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_assertion SIO_000772 20215591 NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_provenance.
- NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_assertion wasDerivedFrom gad-20150221 NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_provenance.
- NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_assertion wasGeneratedBy ECO_0000203 NP91010.RACPTWiFIFy1A3qQoYY941ptSvGAmyqAxkv01ERWwKATo130_provenance.