Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_assertion description "[Phenotypes reconstructed after haplotype analyses showed that the carriers of the combined NAT1 fast+ NAT2 fast phenotypes were at lower risk when compared with those with the combined NAT1 slow + NAT2 slow acetylator phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_assertion evidence source_evidence_literature NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_assertion SIO_000772 17259654 NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_assertion wasDerivedFrom befree-20150227 NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_assertion wasGeneratedBy ECO_0000203 NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP974408.RA5f2Vld1BxhUwNR1YoFjyTs6_frjfAP8MlpfdY_w1mHM130_provenance.