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- source_evidence_literature type ECO_0000212 NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_assertion description "[However, in males, the relatively rare heterozygous genotype GT/(GT) at -663 in the promoter and the variant homozygous genotype G/G at intron 5-5229 appeared to have inverse associations (odds ratio (OR)=0.59, confidence interval (CI): 0.34-1.02 and OR=0.48, CI: 0.24-0.99, respectively), whereas the heterozygous genotype T/C at 3'UTR-8494 had a positive association (OR=1.31, CI: 1.01-1.71) with adenoma development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_assertion evidence source_evidence_literature NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_assertion SIO_000772 16205694 NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_assertion wasDerivedFrom befree-20140225 NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_assertion wasGeneratedBy ECO_0000203 NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP272195.RAcbweD11P8AB97ROyqFTnJOp15k_8eyTWDVDbfxQh2i8130_provenance.