Matches in Nanopublications for { ?s ?p "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 36 of
36
with 100 items per page.
- NP25112.RAd00EGJHeGpjEmXpmIOacS1CYavwxljUsoZFdXBF8_9c130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25112.RAd00EGJHeGpjEmXpmIOacS1CYavwxljUsoZFdXBF8_9c130_provenance.
- NP32389.RAV6CTdKxp0fElkVbWDrd8C-JMNjeWFX8ivCbS79SDJag130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP32389.RAV6CTdKxp0fElkVbWDrd8C-JMNjeWFX8ivCbS79SDJag130_provenance.
- NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP90536.RAvo88DOTTbvK2MLTTi37zkUR3g-X36k4f2PsxOZX_uLY130_provenance.
- NP218527.RAnD3rX_zW3X2UrIdlTcjXQKMAGjLHmGqguHInFhsSB8w130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP218527.RAnD3rX_zW3X2UrIdlTcjXQKMAGjLHmGqguHInFhsSB8w130_provenance.
- NP12736.RAs28UKC7fi1H5X3J7nWGNueVGHIjk_HlrHB5zIovXGqk130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP12736.RAs28UKC7fi1H5X3J7nWGNueVGHIjk_HlrHB5zIovXGqk130_provenance.
- NP91750.RAytXbW6PgiMz6OI4Qe1-qeV_elxpZfhTED8_kQQJ-M-k130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP91750.RAytXbW6PgiMz6OI4Qe1-qeV_elxpZfhTED8_kQQJ-M-k130_provenance.
- NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- NP24899.RAYwon1WrQm8mHqNxFreZXg0qcZksEHxqAmPnJ2R-L-5U130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP24899.RAYwon1WrQm8mHqNxFreZXg0qcZksEHxqAmPnJ2R-L-5U130_provenance.
- NP11346.RAQ1R54b62VdROkeSBDUljD3-cZIlhFn_pCdE3JdoyeiA130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP11346.RAQ1R54b62VdROkeSBDUljD3-cZIlhFn_pCdE3JdoyeiA130_provenance.
- NP89110.RAJxyLbW747LBcLxZx1WegHpupVVIQM--ciCzeEC2-ld4130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89110.RAJxyLbW747LBcLxZx1WegHpupVVIQM--ciCzeEC2-ld4130_provenance.
- NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_provenance.
- NP329471.RA_JCjC8De1qydraN7Fl0Yevf6KsQbZGSUIF6AoUgOquQ130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329471.RA_JCjC8De1qydraN7Fl0Yevf6KsQbZGSUIF6AoUgOquQ130_provenance.
- NP148492.RA0vxGxJ8z-tsOe-hZizvxXhw8uJcDkzEgJwZNhMGDDBE130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP148492.RA0vxGxJ8z-tsOe-hZizvxXhw8uJcDkzEgJwZNhMGDDBE130_provenance.
- NP809669.RACDgC7o2XNaUSdjJ18-orkF75uc1JO3ycX85Q0icRr2Y130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809669.RACDgC7o2XNaUSdjJ18-orkF75uc1JO3ycX85Q0icRr2Y130_provenance.
- NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP32824.RAFpSQNf-k4Qv1Nsqj4f0fvScA3mh0WVyN8_SfqNbYRqw130_provenance.
- assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP26056.RAyQp9sOGmpiPobX62rcvw03emgDah1BB7vLKp72SEdsQ130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26056.RAyQp9sOGmpiPobX62rcvw03emgDah1BB7vLKp72SEdsQ130_provenance.
- NP26058.RA1DpUipxcqGWqddpC_-cCDsPwzDHlrSZkboUmjPO00X0130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26058.RA1DpUipxcqGWqddpC_-cCDsPwzDHlrSZkboUmjPO00X0130_provenance.
- NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809668.RA2fR_v0R5bcmGBst3hFaf067UdQCDI90VYAQW0KD4xlM130_provenance.
- NP143117.RAHCt-nLNsY3PvQkxzCZPFDOn84MZamam1aHt1R4fUFQA130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP143117.RAHCt-nLNsY3PvQkxzCZPFDOn84MZamam1aHt1R4fUFQA130_provenance.
- NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_provenance.
- NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174122.RAdfVy_ecHhtfhJRDNxmlzzzB8-M0VN-EkGS67UqarjVk130_provenance.
- assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_provenance.
- NP158747.RAk_yhMmPDC1I3Vg2-rzbwpZ-pYEMMyzgAb_XTRBrloTE130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP158747.RAk_yhMmPDC1I3Vg2-rzbwpZ-pYEMMyzgAb_XTRBrloTE130_provenance.
- NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP805384.RAIZDZvfF-b-_0YaaObqPeVNYZLXGfE4RtCAmdalc1W-M130_provenance.
- assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP26057.RAPmA4FmSDyGXL8Xv1a0r_5ma_r_7TqOfMq393c6e2c1E130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP26057.RAPmA4FmSDyGXL8Xv1a0r_5ma_r_7TqOfMq393c6e2c1E130_provenance.
- NP174124.RAvnaFALxgIPa_SW0_GSNCnX4xjOgQSU9tSEUR9LmtsJE130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174124.RAvnaFALxgIPa_SW0_GSNCnX4xjOgQSU9tSEUR9LmtsJE130_provenance.
- NP174125.RAp8R-PcFEHTjbdjRr83To3wSyy8d2j6YrxXZrd2vohYA130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174125.RAp8R-PcFEHTjbdjRr83To3wSyy8d2j6YrxXZrd2vohYA130_provenance.
- NP809667.RAs43gTvq8C3mpCuIp8-ueXdOCPUiJSSLHjKeV1EYIhNE130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP809667.RAs43gTvq8C3mpCuIp8-ueXdOCPUiJSSLHjKeV1EYIhNE130_provenance.
- NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_provenance.