Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion> ?p ?o ?g. }
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- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion type Assertion NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_head.
- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion description "[Two variants, 1672C>T in SLC22A4 and -207G>C in SLC22A5, were shown to alter these genes' functions and were identified as genetic susceptibility factors for Crohn's disease (CD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_provenance.
- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion evidence source_evidence_literature NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_provenance.
- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion SIO_000772 16333318 NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_provenance.
- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion wasDerivedFrom gad-20130706 NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_provenance.
- NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_assertion wasGeneratedBy ECO_0000203 NP51659.RAgPFn-AAFzVn-ZVVzuOpRbrfStzgKUVYDRQoLqgRng58130_provenance.