Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.
- 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.
- gad-20130706 importedOn "2013-07-06" NP51670.RAeSjGtLSKVIAqcvMYUaW0WvMzwmZedtNbnJbjVt3w3Tg130_provenance.