Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_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." NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion evidence source_evidence_literature NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion SIO_000772 10719381 NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion wasDerivedFrom befree-20150227 NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_assertion wasGeneratedBy ECO_0000203 NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446690.RAriacKwTjU_RZlRdKociRmpNz10iHFmCIgcgw-1Ru0QM130_provenance.