Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_assertion description "[The finding of a similar prevalence of Cys282Tyr and His63Asp mutations in the HFE gene among controls and patients with coronary atherothrombotic disease, indirectly questions the possibility of an association between hereditary hemochromatosis and atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_assertion evidence source_evidence_literature NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_assertion SIO_000772 10719381 NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_assertion wasDerivedFrom befree-20140225 NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_assertion wasGeneratedBy ECO_0000203 NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP912199.RA5kW4EBYtGrA1Z4N99IdKAVNMip7W6jthMAkL1lfSqBM130_provenance.