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- NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_assertion type Assertion NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_head.
- NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_assertion description "[Missense mutations within the helicase regions of these genes are associated with DNA repair deficiencies and XPD; mutations elsewhere in these genes are correlated with symptoms of XP and Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_provenance.
- NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_assertion evidence source_evidence_literature NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_provenance.
- NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_assertion SIO_000772 10699759 NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_provenance.
- NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_assertion wasDerivedFrom befree-2016 NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_provenance.
- NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_assertion wasGeneratedBy ECO_0000203 NP276882.RApmqCfkzYbj-8v8h7XiMZekts9ZMuS2mBN1JW1vK7yAg130_provenance.