Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_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." NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_assertion evidence source_evidence_literature NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_assertion SIO_000772 17084038 NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_assertion wasDerivedFrom befree-20140225 NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_assertion wasGeneratedBy ECO_0000203 NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP449788.RAxQe-HTzK0bcva42qLIVxcIMceBDxWF4N0C00CQ6MUHI130_provenance.