Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_assertion description "[Recipients carrying the CCR5Delta32 allele developed acute GvHD (grades I-IV) less frequently than did patients lacking the CCR5 deletion mutation (11/35 vs. 76/151, p=0.033).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_assertion evidence source_evidence_literature NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_assertion SIO_000772 17145599 NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_assertion wasDerivedFrom befree-20150227 NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_assertion wasGeneratedBy ECO_0000203 NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP948871.RA4E3O3LfJR-76PlAz-z-fyuf5EwoJRW-LY5wmPMn7jSw130_provenance.