Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_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." NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_assertion evidence source_evidence_literature NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_assertion SIO_000772 12115343 NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_assertion wasDerivedFrom gad-20150221 NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_assertion wasGeneratedBy ECO_0000203 NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.
- gad-20150221 importedOn "2015-02-21" NP75204.RA72dVdMxcJIyckqv4YiKMY-ed3jE0ZJDjKe4adXPXH_Y130_provenance.