Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_assertion> ?p ?o ?g. }
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- NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_assertion type Assertion NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_head.
- NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_assertion description "[The association of the SLC22A -TC haplotype and CARD15 alleles with ileal disease suggests that these variants have biologically intertwined effects in the pathogenesis of CD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.
- NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_assertion evidence source_evidence_literature NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.
- NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_assertion SIO_000772 15685536 NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.
- NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_assertion wasDerivedFrom befree-2016 NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.
- NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_assertion wasGeneratedBy ECO_0000203 NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.