Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_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." NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_assertion evidence source_evidence_literature NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_assertion SIO_000772 25494482 NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_assertion wasDerivedFrom befree-2016 NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_assertion wasGeneratedBy ECO_0000203 NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246775.RAN89CAjXvwwJQh9cy1deFjr3VlKZcoa3koJ5rZTjI3JI130_provenance.