Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_assertion wasGeneratedBy ECO_0000203 NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_assertion wasDerivedFrom befree-2016 NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_assertion SIO_000772 9861324 NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_assertion evidence source_evidence_literature NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.
- NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_assertion description "[We investigated the distribution of this polymorphism, situated at position -318 to the ATG start codon and resulting in a C-T change leading to an Mse I restriction site, in both population based case control studies and family studies in patients with Graves' disease (Caucasian and Hong Kong Chinese), autoimmune hypothyroidism and systemic lupus erythematosus (SLE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1411503.RADmvsXZQOOpK4Wqy6TaOwhHApbCwCMXKIUcXBWJBiNIM130_provenance.