Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_assertion description "[This study provides more stable OR estimates for PCa risk-associated SNPs, which is an important baseline for the effect of these SNPs in risk prediction. These SNPs explain a considerable proportion of genetic variance, however, the majority of genetic variance has yet to be explained.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_assertion evidence source_evidence_literature NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_assertion SIO_000772 20564319 NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_assertion wasDerivedFrom gad-20130706 NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_assertion wasGeneratedBy ECO_0000203 NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.
- gad-20130706 importedOn "2013-07-06" NP50515.RAD__8a2l9QUF3aScgjLVc2JeXZF4UWxNY9Ipgn--HPzM130_provenance.