Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_assertion type Assertion NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_head.
- NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_assertion description "[In total, we identified 78 potentially damaging rare variants (frequency <1%), including ABCA7 p.L400V in a family with Alzheimer's disease and LRRK2 p.R1514Q in 6 of 98 patients with Parkinson's disease (6.1%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_provenance.
- NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_assertion evidence source_evidence_literature NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_provenance.
- NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_assertion SIO_000772 25174650 NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_provenance.
- NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_assertion wasDerivedFrom befree-2016 NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_provenance.
- NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_assertion wasGeneratedBy ECO_0000203 NP1215481.RAPhMKxXNI0FpPRAVfBIer9Cdpw76EIINqllpZxxg5qWg130_provenance.