Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_assertion description "[The GSTM1,GSTT1 and GSTP1 genotype frequencies in two Dutch Caucasian control populations (n = 207 and n = 285) from different but adjacent geographical regions (Maastricht and Nijmegen; distance, 125 km) and 185 patients with HNSCC from the Maastricht region were determined by PCR-related methods.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_assertion evidence source_evidence_literature NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_assertion SIO_000772 16618661 NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_assertion wasDerivedFrom befree-20150227 NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_assertion wasGeneratedBy ECO_0000203 NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP439836.RANuYQB3vpAlP2fLwvZe_QuQVrLEetWNqnOHMmS61nyzQ130_provenance.