Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_assertion description "[IL2-IL21 rs6822844 polymorphism does not appear to be a genetic risk factor for susceptibility to biopsy-proven GCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_assertion evidence source_evidence_literature NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_assertion SIO_000772 21269573 NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_assertion wasDerivedFrom befree-2016 NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_assertion wasGeneratedBy ECO_0000203 NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP867932.RA-ENWCFTQvu1EodPHnmD-mfR_0J0S91zFSqK6kL8bg2Q130_provenance.