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- source_evidence_literature type ECO_0000212 NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion description "[We analyzed the same four 5' FCRL3 single nucleotide polymorphism markers, together with three additional exonic single nucleotide polymorphisms in the FCRL3 gene, in cohorts of white Caucasians with Graves' disease (n = 625), type 1 diabetes (n = 279), autoimmune Addison's disease (AAD; n = 200), and RA (n = 769).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion evidence source_evidence_literature NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion SIO_000772 17200162 NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion wasDerivedFrom befree-2016 NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_assertion wasGeneratedBy ECO_0000203 NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.
- befree-2016 importedOn "2016-02-19" NP586825.RADLUAWfJvActCQLCP_UIhNd-yPnA4JdRDjPTsHrirp1I130_provenance.