Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_assertion description "[There were no differences in the frequencies of the GSTM1 and GSTT1 null genotypes, and the slow acetylator genotype, between hypersensitive and non-sensitive patients, while GSTP1 frequency was lower (although non-significant) in the hypersensitive group [21% versus 32%, odds ratio (OR) = 0.5, Pc = 0.24].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_assertion evidence source_evidence_literature NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_assertion SIO_000772 11186133 NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_assertion wasDerivedFrom befree-20150227 NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_assertion wasGeneratedBy ECO_0000203 NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP441043.RA6JLngb1cp9rRE2Zj7VIF_3udmRqmVW0tD6TV2PD4r4k130_provenance.