Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_assertion description "[this is the first evidence that the association between the frequencies of GST-M1 and GST-T1 null genotypes & Behcet's disease might be dependent on the interaction of multiple null allele polymorphisms rather than a single null allele of GST-M1 & GST-T1 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_assertion evidence source_evidence_literature NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_assertion SIO_000772 16283344 NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_assertion wasDerivedFrom lhgdn-20090331 NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_assertion wasGeneratedBy ECO_0000203 NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP195852.RAOBzKecZgWKQ2IgLTmQDNsaZtyevkS_ugKMSLbLKKesA130_provenance.