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- source_evidence_literature type ECO_0000212 NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion description "[Among the subjects in our study groups, including patients with CD, UC and healthy controls, none had OCTN and CARD15 variants and very rare IBD family history was found in our patients with the percentage of 0 (0/61 with CD) and 1.3% (2/151 with UC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion evidence source_evidence_literature NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion SIO_000772 18756601 NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion wasDerivedFrom befree-2016 NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_assertion wasGeneratedBy ECO_0000203 NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.
- befree-2016 importedOn "2016-02-19" NP690383.RA_j9VKHmdbftltcnoZQjRb8HfSv_HYnBuzTsj3-Izh6E130_provenance.