Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_assertion description "[CD susceptibility polymorphisms ATG16L1 rs2241880, ICAM1 rs5498, IL4 rs2070874, IL17F rs763780, IRGM rs13361189, ITLN1 rs2274910, LRRK2 rs11175593, and TLR4 rs4986790 were genotyped in a Portuguese population (511 CD patients, 626 controls) and assessed for association with CD clinical characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_assertion evidence source_evidence_literature NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_assertion SIO_000772 22573572 NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_assertion wasDerivedFrom befree-20140225 NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_assertion wasGeneratedBy ECO_0000203 NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP761819.RAjd66nzef6dmB2e6Q8PyaZbqdfL3VrGT7nsqEJdECA8M130_provenance.