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- NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_assertion type Assertion NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_head.
- NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_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." NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_provenance.
- NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_assertion evidence source_evidence_literature NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_provenance.
- NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_assertion SIO_000772 17145599 NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_provenance.
- NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_assertion wasDerivedFrom befree-20140225 NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_provenance.
- NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_assertion wasGeneratedBy ECO_0000203 NP301258.RA_YHq8LPa7hKzxU1PyzK5Z9rPBTsqmut7-Dp9mOoVCWI130_provenance.