Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_assertion description "[In conclusion, our results reveal a great diversity for KIR genotypes in donors and recipients of BMT and that the risk of GVHD was maximum in unrelated BMT when the recipient KIR genotype was `included` in the donor KIR genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_assertion evidence source_evidence_literature NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_assertion SIO_000772 12039408 NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_assertion wasDerivedFrom gad-20130706 NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_assertion wasGeneratedBy ECO_0000203 NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.
- gad-20130706 importedOn "2013-07-06" NP61119.RAiYJeI9JVNPkevMfeDxF8oM9MhhZUPYbwSu0uxel_w_s130_provenance.