Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_assertion> ?p ?o ?g. }
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- NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_assertion type Assertion NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_head.
- NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_assertion description "[Phenotype-genotype associations were evaluated in a Canadian cohort including 507 patients with CD, 216 patients with UC, and 352 ethnically matched controls genotyped for SLC22A4 C1672T, SLC22A5 G-207C, and the major CD-associated CARD15 variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_provenance.
- NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_assertion evidence source_evidence_literature NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_provenance.
- NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_assertion SIO_000772 15685536 NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_provenance.
- NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_assertion wasDerivedFrom gad-20150221 NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_provenance.
- NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_assertion wasGeneratedBy ECO_0000203 NP90368.RAI9FRBv1S5k9F9bjIOD46Afhriv8MqehPQG2R2vczrTM130_provenance.