Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_assertion description "[Patients carrying at least one variant allele of XPD rs1799793 had a reduced risk of developing osteosarcoma, compared with wild-type patients (odds ratio = 0.55, 95% CI 0.36-0.84).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_assertion evidence source_evidence_literature NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_assertion SIO_000772 21826087 NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_assertion wasDerivedFrom befree-20140225 NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_assertion wasGeneratedBy ECO_0000203 NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP236501.RAN5n04TV784BykdgULm1kDbiPc86dx-isWx90oD6j1sI130_provenance.