Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_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." NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_assertion evidence source_evidence_curated NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_assertion SIO_000772 21292315 NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_assertion wasDerivedFrom gwascat-2016 NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_assertion wasGeneratedBy ECO_0000218 NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP52649.RA7CeriwGspBSAa3zSJfFoA2ChBqXZMJ8J_Cf-uC1SK2Q130_provenance.