Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_assertion> ?p ?o ?g. }
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- NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_assertion type Assertion NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_head.
- NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_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." NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_provenance.
- NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_assertion evidence source_evidence_literature NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_provenance.
- NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_assertion SIO_000772 17145599 NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_provenance.
- NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_assertion wasDerivedFrom befree-2016 NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_provenance.
- NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_assertion wasGeneratedBy ECO_0000203 NP582452.RAWLwgti9mfDqGukxhCmuQyOww7Zs6u9Jm8xg7CVmbB7o130_provenance.