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- NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_assertion type Assertion NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_head.
- NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_assertion description "[The association of mutations in RDS with retinitis pigmentosa indicates that ROM1 is a strong candidate gene for human retinopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_provenance.
- NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_assertion evidence source_evidence_literature NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_provenance.
- NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_assertion SIO_000772 1610568 NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_provenance.
- NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_assertion wasDerivedFrom befree-20140225 NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_provenance.
- NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_assertion wasGeneratedBy ECO_0000203 NP584923.RAG5_ppWWcXFIqzerPKvJBdCEh8WmKjgdZvdbch9FHsmM130_provenance.