Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_assertion description "[A case-control study (575 morbidly obese and 646 control subjects) analyzing GAD2 variants identified both a protective haplotype, including the most frequent alleles of single nucleotide polymorphisms (SNPs) +61450 C>A and +83897 T>A (OR = 0.81, 95% CI [0.681-0.972], p = 0.0049) and an at-risk SNP (-243 A>G) for morbid obesity (OR = 1.3, 95% CI [1.053-1.585], p = 0.014).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_assertion evidence source_evidence_literature NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_assertion SIO_000772 14691540 NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_assertion wasDerivedFrom befree-2016 NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_assertion wasGeneratedBy ECO_0000203 NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.
- befree-2016 importedOn "2016-02-19" NP425809.RAG1sMccWv0Cg5l4s7YW-u-bI8L6Qu0ID5nYA0hxLpix0130_provenance.