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- source_evidence_literature type ECO_0000212 NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_assertion description "[In contrast, mutations in two members of the TFIIH complex, the XPB and XPD genes are generally very severe with both skin and CNS disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_assertion evidence source_evidence_literature NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_assertion SIO_000772 10699759 NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_assertion wasDerivedFrom befree-20140225 NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_assertion wasGeneratedBy ECO_0000203 NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_provenance.