Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_assertion> ?p ?o ?g. }
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- NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_assertion type Assertion NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_head.
- NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_assertion wasGeneratedBy ECO_0000203 NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_provenance.
- NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_assertion wasDerivedFrom gad-20150221 NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_provenance.
- NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_assertion SIO_000772 20436471 NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_provenance.
- NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_assertion evidence source_evidence_literature NP174123.RAH3aYBEzGCFGR6re8NzygaACgRKn8mjoXbIHOqmeAvAg130_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.