Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_assertion> ?p ?o ?g. }
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- NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_assertion type Assertion NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_head.
- NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_assertion wasGeneratedBy ECO_0000203 NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_provenance.
- NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_assertion wasDerivedFrom befree-2016 NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_provenance.
- NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_assertion SIO_000772 25581431 NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_provenance.
- NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_assertion evidence source_evidence_literature NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_provenance.
- NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_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." NP1254787.RAda2-mTuzYcZSsK9L7OAK2Uq7IuEF2igQRVc79W1VdwI130_provenance.