Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_assertion> ?p ?o ?g. }
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- NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_assertion type Assertion NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_head.
- NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_assertion description "[Cockayne syndrome (CS) is mainly caused by mutations in the Cockayne syndrome group A or B (CSA or CSB) genes which are required for a sub-pathway of nucleotide excision repair entitled transcription coupled repair.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_provenance.
- NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_assertion evidence source_evidence_literature NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_provenance.
- NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_assertion SIO_000772 17084038 NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_provenance.
- NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_assertion wasDerivedFrom befree-20140225 NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_provenance.
- NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_assertion wasGeneratedBy ECO_0000203 NP691370.RA8qRq4kYiUSRINc9D_RqqlYNN1taUlzwiG-JzFKgVfzg130_provenance.