Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion type Assertion NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_head.
- NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion wasGeneratedBy ECO_0000203 NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance.
- NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion wasDerivedFrom befree-2016 NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance.
- NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion SIO_000772 25581431 NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance.
- NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion evidence source_evidence_literature NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance.
- NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_assertion description "[Variants at 1p36 (nearest gene, WNT4), 4q26 (SYNPO2), 9q34.2 (ABO) and 17q11.2 (ATAD5) were associated with EOC risk, and at 1p34.3 (RSPO1) and 6p22.1 (GPX6) variants were specifically associated with the serous EOC subtype, all with P < 5 × 10(-8).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1254794.RAPjBInzabTanPKkjgo1jn6QZsqSm5Y1R7NVcLLW8GOC0130_provenance.