Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_assertion> ?p ?o ?g. }
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- NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_assertion type Assertion NP92022.RAF1EQAG8f-FrRzITadIjVht-mfkGThv5R1IGoKi3LFMQ130_head.
- 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.