Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.
- 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.
- gwascat-2016 importedOn "2016-01-27" NP52645.RAvveI2evBFf4rylQMXnzKQNFIUQngLx-wmK9WRPx4gVM130_provenance.