Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_assertion wasGeneratedBy ECO_0000203 NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_assertion wasDerivedFrom befree-2016 NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_assertion SIO_000772 25581431 NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_assertion evidence source_evidence_literature NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.
- NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_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." NP1254796.RA0fQKUuFZNTi0BtkPpns-T21mbHle7oE39BKHVP46sMw130_provenance.