Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_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." NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_assertion evidence source_evidence_literature NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_assertion SIO_000772 17145599 NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_assertion wasDerivedFrom befree-20140225 NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_assertion wasGeneratedBy ECO_0000203 NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404371.RAO937Q0Z3ZmuRx1_sb06ISGDJTryfZei5aNx7jBKXaJQ130_provenance.