Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_assertion description "[The present study investigated the genetic variation of 3' flanking region of ApoA-I (PstI), 3' untranslated region of ApoC-III (SstI) and intron 2 of ApoA-IV (XbaI) in 193 angiographically diagnosed CHD patients and 150 CHD negative controls of Punjab, Northwest India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_assertion evidence source_evidence_literature NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_assertion SIO_000772 17825930 NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_assertion wasDerivedFrom gad-20150221 NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_assertion wasGeneratedBy ECO_0000203 NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76543.RAXqX8atNccTeOZHuBtU9uH0NuqbgKmKc2j3ZxG62y_GY130_provenance.