Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_assertion wasGeneratedBy ECO_0000203 NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_assertion wasDerivedFrom gad-20150221 NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_assertion SIO_000772 17719079 NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_assertion evidence source_evidence_literature NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.
- NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_assertion description "[MTHFR C677T mutation in central retinal vein occlusion: a case-control study in Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_provenance.