Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_assertion type Assertion NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_head.
- NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_assertion description "[Blau syndrome is a monogenic disease resulting from mutations in the pattern recognition receptor NOD2, and is phenotypically characterized by the triad of granulomatous polyarthritis, dermatitis and uveitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.
- NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_assertion evidence source_evidence_literature NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.
- NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_assertion SIO_000772 25136265 NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.
- NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_assertion wasDerivedFrom befree-2016 NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.
- NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_assertion wasGeneratedBy ECO_0000203 NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.