Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_assertion description "[Recently, two studies have reported association of single-nucleotide polymorphism (SNP) rs31480 in interleukin 3 (IL-3) and the rs1368408 and SNP75 (-623 approximately -622 AG/-T) SNPs in secretoglobulin family 3a member 2 (SCGB3A2) with GD and suggested that this may account for linkage to the 5q31-33 region in Oriental GD datasets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_assertion evidence source_evidence_literature NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_assertion SIO_000772 20210668 NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_assertion wasDerivedFrom befree-20150227 NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_assertion wasGeneratedBy ECO_0000203 NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP494244.RAeuZE8KF29NlrRA3Hpb4eQiu871-KfvK1hnOj7Y2I0fk130_provenance.