Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_assertion description "[Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_assertion evidence source_evidence_curated NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_assertion SIO_000772 21685912 NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_assertion wasDerivedFrom gwascat-2016 NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_assertion wasGeneratedBy ECO_0000218 NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP52907.RAyXEPyviW-QeiXFVcVCCsSVQ_0DBlLAVE67z3Ea2JAvk130_provenance.