Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_assertion description "[The HLA molecule most likely to be involved in coeliac disease is a specific DQ alpha/DQ beta heterodimer, encoded in cis arrangement in DR3 haplotypes or in trans arrangement in a DR5, 7 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_assertion evidence source_evidence_literature NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_assertion SIO_000772 1674926 NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_assertion wasDerivedFrom befree-20140225 NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_assertion wasGeneratedBy ECO_0000203 NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP212377.RAdryBYLybfWfZoSsvaZIdf4Y6JIIMMfGn2VSVaP8lHSE130_provenance.