Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP478863.RAcJ1k1-ildd_MsOQ2Pq9d-XtHUOs8KLR7WFhbNwKWQqk130_provenance.