Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_assertion> ?p ?o ?g. }
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- NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_assertion type Assertion NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_head.
- NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_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." NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_provenance.
- NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_assertion evidence source_evidence_literature NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_provenance.
- NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_assertion SIO_000772 17084038 NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_provenance.
- NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_assertion wasDerivedFrom befree-2016 NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_provenance.
- NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_assertion wasGeneratedBy ECO_0000203 NP577727.RANW1ubO7vZoi9skDVE4E2G_B2VoHKfdL3-cUfdpLNV0o130_provenance.