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- source_evidence_literature type ECO_0000212 NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_assertion description "[We investigated disease phenotype association to genetic variations in IL23R, ATG16L1, DLG5, ABCB1/MDR1, TLR4, TNFRSF1A, chromosome 5 risk haplotype including SLC22A4 and SLC22A5, and HLA-DRB1*0103 allele among Finnish IBD patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_assertion evidence source_evidence_literature NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_assertion SIO_000772 18338763 NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_assertion wasDerivedFrom gad-20150221 NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_assertion wasGeneratedBy ECO_0000203 NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP120214.RAiD4M9S4Pz7a8vuIUk9xjgH5AYpjU7p_lt1XFmXEevpE130_provenance.