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- source_evidence_literature type ECO_0000212 NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_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." NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_assertion evidence source_evidence_literature NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_assertion SIO_000772 17200162 NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_assertion wasDerivedFrom befree-20150227 NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_assertion wasGeneratedBy ECO_0000203 NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP965526.RAP9b5dJE1_sAMgsuWWvLoHzfTgdpSxuN2IZLZwxBPGsc130_provenance.