Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- 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.
- NP1254792.RAS2v_r5BSzYvQhvu03GTNEXHn6-jv7SYQItvYuE0mZKA130_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." NP1254792.RAS2v_r5BSzYvQhvu03GTNEXHn6-jv7SYQItvYuE0mZKA130_provenance.
- NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_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." NP55514.RAqj5_tS02t2sNqY8b_E21HHra89eWkmoyoQezENyL1ec130_provenance.
- NP1254798.RAt8VbDqHlXJHefCiAPZGnrSnkOpQu3Vp5wMwbAZxROco130_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." NP1254798.RAt8VbDqHlXJHefCiAPZGnrSnkOpQu3Vp5wMwbAZxROco130_provenance.
- NP1254790.RAJS6IwQg43lpN7er3ZO0ClLgFfNLEOuuppf_wFIVLvu0130_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." NP1254790.RAJS6IwQg43lpN7er3ZO0ClLgFfNLEOuuppf_wFIVLvu0130_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.
- 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.
- NP55521.RAzIg8yn3soeJ_CaZQhGwd2BK3cR8wUBS5joMWqyysaDU130_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." NP55521.RAzIg8yn3soeJ_CaZQhGwd2BK3cR8wUBS5joMWqyysaDU130_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.