Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_assertion description "[Furthermore, MTHFR C677T homozygosity was not associated with increased risk of ICD or VTE in subgroups after stratification for sex, age, cholesterol, high-density lipoprotein cholesterol, lipoprotein(a), fibrinogen, triglycerides, body mass index, smoking, diabetes mellitus, hypertension, and factor V Leiden genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_assertion evidence source_evidence_literature NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_assertion SIO_000772 15226189 NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_assertion wasDerivedFrom befree-20140225 NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_assertion wasGeneratedBy ECO_0000203 NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP285810.RAYi_pLtZR95Q4L_vd_b4AdtkQm5m8papoIK_Au9g4MQM130_provenance.