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- source_evidence_literature type ECO_0000212 NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_assertion description "[In the combined analysis, risk of TGCT was significantly associated with markers at four previously unreported loci: 4q22.2 in HPGDS (per-allele odds ratio (OR) = 1.19, 95% confidence interval (CI) = 1.12-1.26; P = 1.11 � 10(-8)), 7p22.3 in MAD1L1 (OR = 1.21, 95% CI = 1.14-1.29; P = 5.59 � 10(-9)), 16q22.3 in RFWD3 (OR = 1.26, 95% CI = 1.18-1.34; P = 5.15 � 10(-12)) and 17q22 (rs9905704: OR = 1.27, 95% CI = 1.18-1.33; P = 4.32 � 10(-13) and rs7221274: OR = 1.20, 95% CI = 1.12-1.28; P = 4.04 � 10(-9)), a locus that includes TEX14, RAD51C and PPM1E.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_assertion evidence source_evidence_literature NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_assertion SIO_000772 23666239 NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_assertion wasDerivedFrom befree-20150227 NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_assertion wasGeneratedBy ECO_0000203 NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP889008.RAaLT69ohtn9aLTLs-aLXteoul102b6qIM21POqS8TPp4130_provenance.