Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_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." NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_assertion evidence source_evidence_literature NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_assertion SIO_000772 12927690 NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_assertion wasDerivedFrom befree-2016 NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_assertion wasGeneratedBy ECO_0000203 NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.
- befree-2016 importedOn "2016-02-19" NP406084.RA-B1HUQPDDtD4c0V3II0ajriSgeJqsCjlxQP6FkRXErA130_provenance.