Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_assertion type Assertion NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_head.
- NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_assertion description "[Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.
- NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_assertion evidence source_evidence_curated NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.
- NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_assertion SIO_000772 21292315 NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.
- NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_assertion wasDerivedFrom gwascat-2016 NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.
- NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_assertion wasGeneratedBy ECO_0000218 NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.