Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_assertion description "[To determine the association between GSTM1 and GSTT1 homozygous deletions (GSTM1 null and GSTT1 null, respectively) and CMM, we studied 212 patients with CMM, 150 patients with CMM and dysplastic nevi (DN), 147 patients with DN alone, and 124 healthy persons without CMM or DN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_assertion evidence source_evidence_literature NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_assertion SIO_000772 11352862 NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_assertion wasDerivedFrom befree-20140225 NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_assertion wasGeneratedBy ECO_0000203 NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435206.RArL4uvYZn1wj4CTgTIIY1sSTC6SDq8t7fyDiNNyASMw0130_provenance.