Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1414860.RA5c_jgYiMLRjHy4a5vaKj_rFBrCJvW3YVL9ZJ-oHSk4w#provenance>. }
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- source_evidence_curated type ECO_0000205 provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." provenance.
- CTD_human importedOn "2017-01-25" provenance.
- assertion wasGeneratedBy ECO_0000218 provenance.
- assertion wasDerivedFrom CTD_human provenance.
- assertion SIO_000772 25581431 provenance.
- assertion evidence source_evidence_curated provenance.
- 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." provenance.