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- source_evidence_literature type ECO_0000212 NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion description "[Although XPD (A-751G), XRCC1 (A399G), and XRCC4 (G-1394T) gene polymorphisms have been extensively investigated in different clinical pictures, this is the first study to evaluate the role of these polymorphisms in the genetic etiopathogenesis of RA in Turkish patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion evidence source_evidence_literature NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion SIO_000772 25494482 NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion wasDerivedFrom befree-2016 NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_assertion wasGeneratedBy ECO_0000203 NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246773.RAOSK8VBoiCm50oK0lFq98Sl5MRVXxzKUvrDB046swuso130_provenance.