Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_assertion> ?p ?o ?g. }
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- NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_assertion type Assertion NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_head.
- NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_assertion wasGeneratedBy ECO_0000203 NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_provenance.
- NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_assertion wasDerivedFrom befree-20150227 NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_provenance.
- NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_assertion SIO_000772 20436471 NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_provenance.
- NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_assertion evidence source_evidence_literature NP836996.RAA5F_zsGVHg0PMkDE6Tiogg5cZpGcuhhs_KEP9vi7iTA130_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.