Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_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." NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_assertion evidence source_evidence_literature NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_assertion SIO_000772 20173792 NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_assertion wasDerivedFrom befree-20150227 NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_assertion wasGeneratedBy ECO_0000203 NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP407088.RAWlmjsYdO5JcxH7Auv3quXSe9mM25IKWTMi34CHOSv-E130_provenance.