Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_assertion description "[Individuals carrying 3-4 risk genotypes in MDM2 and p14(ARF) were at increased SGC risk (OR, 2.0, 95% CI, 1.1-2.7) compared with individuals carrying 0-2 risk genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_assertion evidence source_evidence_literature NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_assertion SIO_000772 23145162 NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_assertion wasDerivedFrom befree-20140225 NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_assertion wasGeneratedBy ECO_0000203 NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP549332.RAqKwvEn0BZrLc9Miu9g_r5MqkhbZdeYdirAHEPFyp3eU130_provenance.