Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_assertion description "[Our study suggests that KIR genotyping of donor and recipient pairs could contribute to the identification of patients at high risk for developing severe complications of haematopoietic SCT and thus may help with the choice of intensity of GVHD prophylaxis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_assertion evidence source_evidence_literature NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_assertion SIO_000772 20173792 NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_assertion wasDerivedFrom befree-20150227 NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_assertion wasGeneratedBy ECO_0000203 NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683709.RALRq1qs-mhFSl-YXdG_H2aFPZL6IBhVTfkguzyWrm_sU130_provenance.