Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_assertion description "[Genetic variation in p53 and ATM haplotypes and risk of glioma and meningioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_assertion evidence source_evidence_literature NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_assertion SIO_000772 17151932 NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_assertion wasDerivedFrom befree-20140225 NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_assertion wasGeneratedBy ECO_0000203 NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP522601.RACs8LBd9oSpSi_RrCBx55XpKWob4B2wMing6088rw5Oo130_provenance.