Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_assertion description "[NOD2 polymorphism screening should be used to optimize donor selection and antimicrobial prophylaxis to reduce the occurrence of aGVHD and TRM following allogeneic HSCT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_assertion evidence source_evidence_literature NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_assertion SIO_000772 19219079 NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_assertion wasDerivedFrom gad-20150221 NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_assertion wasGeneratedBy ECO_0000203 NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP86611.RAkdGpDl_jCHLBgpghApsdTBtCBqdxRCzle7Zhmxg74Wk130_provenance.