Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_assertion description "[The aim of this study was to investigate the frequency of C677T methylenetetrahydrofolate reductase (MTHFR) mutation in healthy Croatian volunteers and in patients with atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_assertion evidence source_evidence_literature NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_assertion SIO_000772 12927690 NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_assertion wasDerivedFrom gad-20150221 NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_assertion wasGeneratedBy ECO_0000203 NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP81312.RA1NnWg-hWlvp-z-JjowM_Lz4YoNvsjGdMUzN6XBGGjtE130_provenance.