Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_assertion description "[This paper provides a concise review of the 24 published studies that evaluated the risk of SCCHN in relation to two deletion polymorphisms of the glutathione S-transferase family: GSTM1 and GSTT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_assertion evidence source_evidence_literature NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_assertion SIO_000772 11447041 NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_assertion wasDerivedFrom befree-20150227 NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_assertion wasGeneratedBy ECO_0000203 NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP888979.RALnmPcUhqXPGgRGnXIrPyyEYjBEkk54_YVxNOebTZ_fM130_provenance.