Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_assertion description "[In addition, this study is one of the largest GST polymorphism studies undertaken in the Spanish population and the first time that copy number variants have been scrutinized in relation to MM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_assertion evidence source_evidence_literature NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_assertion SIO_000772 22251241 NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_assertion wasDerivedFrom befree-20150227 NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_assertion wasGeneratedBy ECO_0000203 NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP988120.RA1SasiRWq8tkoQoBd9gkjAVG2gEaiyE6nFO3OcW2XXfM130_provenance.