Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_assertion> ?p ?o ?g. }
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- NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_assertion type Assertion NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_head.
- NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_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." NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_provenance.
- NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_assertion evidence source_evidence_curated NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_provenance.
- NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_assertion SIO_000772 21292315 NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_provenance.
- NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_assertion wasDerivedFrom gwascat-2016 NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_provenance.
- NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_assertion wasGeneratedBy ECO_0000218 NP52647.RAQz_1OyjjlNpeLS1PMRtrAzUXe_Lcpc23GIyx17fiHJA130_provenance.