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- NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_assertion type Assertion NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_head.
- NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_assertion wasGeneratedBy ECO_0000203 NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_provenance.
- NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_assertion wasDerivedFrom gad-20150221 NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_provenance.
- NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_assertion SIO_000772 20436471 NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_provenance.
- NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_assertion evidence source_evidence_literature NP146049.RApWTvlxspN0I_wkfFtebuNvPj6zRmUmI6DgC4Ij6tEbg130_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.