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- NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_assertion type Assertion NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_head.
- NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_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." NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_provenance.
- NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_assertion evidence source_evidence_literature NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_provenance.
- NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_assertion SIO_000772 10699759 NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_provenance.
- NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_assertion wasDerivedFrom befree-2016 NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_provenance.
- NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_assertion wasGeneratedBy ECO_0000203 NP276878.RAENsxQFUk0FI1SbjLvW_nGk-xfF6Ez2iGmO1x5kjqi-I130_provenance.