Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_assertion wasGeneratedBy ECO_0000203 NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_assertion wasDerivedFrom befree-20140225 NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_assertion SIO_000772 17712558 NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_assertion evidence source_evidence_literature NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_assertion description "[Our data demonstrated that Saudi individuals carrying MTHFR genotype 1298CC (p < 0.001) and the 1298C allele (p = 0.012) had 4.23 and 1.73-fold higher risk of developing DLBCL, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP376634.RAfdcNnxOa0u3zkVCU9RgBtJ8nP8S0iYmH7AY_73ioGvw130_provenance.