Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1211860.RAmM5g3JSBcn6Tdy0H15gZpUiRifl4dxhGDCiP5cZrKdo130_provenance.