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- source_evidence_literature type ECO_0000212 NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_assertion description "[The Arg389Gly polymorphism in the ADRB1 gene showed significantly different allele and genotype frequencies in patients with NTG than in controls (p = 0.004 and 0.006, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_assertion evidence source_evidence_literature NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_assertion SIO_000772 16785856 NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_assertion wasDerivedFrom befree-20150227 NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_assertion wasGeneratedBy ECO_0000203 NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP226724.RACgBUieuINqT7drJBlNY4Ed9CjeP5Bet6Vn1Y6C97t0k130_provenance.