Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_assertion description "[The prevalence of the factor V Leiden mutation (FVL) and the prothrombin G20210A mutation and of homozygosity for the methylenetetrahydrofolate reductase (MTHFR) C677T substitution has been analyzed in a cohort of 175 patients with gastrointestinal adenocarcinoma by the polymerase chain reaction-restriction fragment length polymorphism technique.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_assertion evidence source_evidence_literature NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_assertion SIO_000772 12115343 NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_assertion wasDerivedFrom befree-20140225 NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_assertion wasGeneratedBy ECO_0000203 NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP528896.RA4uVS7h8iYh2gNM2pRQIsBTtTTA_GbGVfaoYbT3EyEr0130_provenance.