<http://www.reactome.org/biopax/48892Evidence772> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.biopax.org/release/biopax-level3.owl#Evidence> .
<http://www.reactome.org/biopax/48892Evidence772> <http://www.biopax.org/release/biopax-level3.owl#comment> "After the primers are synthesized, Replication Factor C binds to the 3'-end of the initiator DNA to trigger polymerase switching. The non-processive nature of pol alpha catalytic activity and the tight binding of Replication Factor C to the primer-template junction presumably lead to the turnover of the pol alpha:primase complex. After the Pol alpha-primase primase complex is displaced from the primer, the proliferating cell nuclear antigen (PCNA) binds to form a \"sliding clamp\" structure. Replication Factor C then dissociates, and DNA polymerase delta binds and catalyzes the processive synthesis of DNA."^^<http://www.w3.org/2001/XMLSchema#string> .
<http://www.reactome.org/biopax/48892Evidence772> <http://www.biopax.org/release/biopax-level3.owl#xref> <http://identifiers.org/pubmed/1671046> .
<http://www.reactome.org/biopax/48892Evidence772> <http://www.biopax.org/release/biopax-level3.owl#xref> <http://identifiers.org/pubmed/1670772> .
<http://www.reactome.org/biopax/48892Evidence772> <http://www.biopax.org/release/biopax-level3.owl#xref> <http://identifiers.org/pubmed/1967833> .
<http://www.reactome.org/biopax/48892Evidence772> <http://www.biopax.org/release/biopax-level3.owl#evidenceCode> <http://www.reactome.org/biopax/48892EvidenceCodeVocabulary1> .