Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_assertion> ?p ?o ?g. }
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- NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_assertion type Assertion NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_head.
- NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_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." NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_assertion evidence source_evidence_literature NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_assertion SIO_000772 16333318 NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_assertion wasDerivedFrom gad-20130706 NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_assertion wasGeneratedBy ECO_0000203 NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.