Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_assertion> ?p ?o ?g. }
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- NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_assertion type Assertion NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_head.
- NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_assertion wasGeneratedBy ECO_0000218 NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_provenance.
- NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_assertion wasDerivedFrom gwascat-2016 NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_provenance.
- NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_assertion SIO_000772 20436471 NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_provenance.
- NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_assertion evidence source_evidence_curated NP52347.RAaqiKk389UsAJRd9qzQmicxKet6nvAAAag5_iWrw0684130_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.