Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_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." NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion evidence source_evidence_curated NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion SIO_000772 25581431 NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion wasDerivedFrom gwascat-2016 NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_assertion wasGeneratedBy ECO_0000218 NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.
- gwascat-2016 importedOn "2016-01-27" NP55517.RA-yt2srywylLEb63EnCd1kUbQMudKRd9PUMBL9sWB_5Q130_provenance.