Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_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." NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_assertion evidence source_evidence_literature NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_assertion SIO_000772 15848047 NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_assertion wasDerivedFrom befree-20140225 NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_assertion wasGeneratedBy ECO_0000203 NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP615781.RAjWGrxZXEC37a31lKHFqeJfb4Yg3v4YXQWMa6MzM_9Sk130_provenance.