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- source_evidence_literature type ECO_0000212 NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_assertion description "[There was a significant decrease in coronary artery disease incidence in patients carrying a CYP2E1*6 genetic polymorphism (39.7% of the noncarriers vs. 13.6% of the carriers had coronary artery disease; p = 0.019); similar results were found with the haplotype analysis (p = 0.03) but not with CYP2E1*5B alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_assertion evidence source_evidence_literature NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_assertion SIO_000772 20406102 NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_assertion wasDerivedFrom befree-20140225 NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_assertion wasGeneratedBy ECO_0000203 NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP885831.RAL-HwLCN7OK1tz2hHL8m6yJhoW8vhFf_KbHcWeHp4TIA130_provenance.