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- source_evidence_literature type ECO_0000212 NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- befree-2016 importedOn "2016-02-19" NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_assertion wasGeneratedBy ECO_0000203 NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_assertion wasDerivedFrom befree-2016 NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_assertion SIO_000772 22286173 NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_assertion evidence source_evidence_literature NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.
- NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_assertion description "[Additionally, we successfully replicated and validated rs10757272 on CDKN2BAS at chromosome 9p21.3 (combined P-value = 1.55 × 10(-7); odds ratio = 1.21) to be significantly associated with IA as previously reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP956731.RAnjVY7Hvm3WWaP4mrXlcUYIIAIDkY6tic31W1Vm6VoTE130_provenance.