Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_assertion description "[We compared the GSTT1, GSTM1 and GSTP1 genotype frequencies in two groups of healthy blood donors, collected from different but adjacent regions in the Netherlands, with those of a group of patients with HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_assertion evidence source_evidence_literature NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_assertion SIO_000772 16618661 NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_assertion wasDerivedFrom befree-20140225 NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_assertion wasGeneratedBy ECO_0000203 NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.
- befree-20140225 importedOn "2014-02-25" NP489387.RAO-dpeXfHaWmXsCioy0DpKcHM6Pk7QBE7zhT6Vt-M4v4130_provenance.