Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_assertion> ?p ?o ?g. }
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- NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_assertion type Assertion NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_head.
- NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_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." NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_provenance.
- NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_assertion evidence source_evidence_literature NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_provenance.
- NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_assertion SIO_000772 17084038 NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_provenance.
- NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_assertion wasDerivedFrom befree-20140225 NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_provenance.
- NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_assertion wasGeneratedBy ECO_0000203 NP325136.RAr8wIMfPxDmlFvfFf_Xt_KMgpum950U7ZEtK5b9heddM130_provenance.