Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion description "[In view of the emerging role of polymorphic variants in complex diseases and minimizing of possible confounding factors in this association study, we conclude that allelic variation in the NRAMP1 promoter may contribute significantly to MS susceptibility in the South African Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion evidence source_evidence_literature NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion SIO_000772 11358358 NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion wasDerivedFrom befree-20140225 NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion wasGeneratedBy ECO_0000203 NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance.