Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_assertion description "[G/A1180 dimorphism and two other SNPs, C/T771 TBP and G/T(-271) PDCD2, were shown to share three common haplotypes, two of which (A-T-G and A-T-T) have been associated with higher development risk of T1D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_assertion evidence source_evidence_literature NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_assertion SIO_000772 15848047 NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_assertion wasDerivedFrom gad-20150221 NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_assertion wasGeneratedBy ECO_0000203 NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92114.RApQTkvobmhnd-2_RW4-BKOz4wfQk9bLkGI0gU9W_hNpM130_provenance.