Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_assertion type Assertion NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_head.
- NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_assertion description "[After imputation to 1000 Genomes Project data, we assessed associations of 11 million genetic variants with EOC risk from 15,437 cases unselected for family history and 30,845 controls and from 15,252 BRCA1 mutation carriers and 8,211 BRCA2 mutation carriers (3,096 with ovarian cancer), and we combined the results in a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_provenance.
- NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_assertion evidence source_evidence_literature NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_provenance.
- NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_assertion SIO_000772 25581431 NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_provenance.
- NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_assertion wasDerivedFrom befree-2016 NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_provenance.
- NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_assertion wasGeneratedBy ECO_0000203 NP1254788.RAgvtvjCKIRct8zpe-2rX-JfGwtbQHRro9nP3F5e8fmt0130_provenance.