Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_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." NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion evidence source_evidence_literature NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion SIO_000772 20173792 NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion wasDerivedFrom befree-20140225 NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_assertion wasGeneratedBy ECO_0000203 NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP216806.RA0glauviSFSEbpTm2psA1jJdFUSQq1r3S6rigA3eDauA130_provenance.