Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_assertion type Assertion NP565028.RAJtBchd92S5jFqOW3irPKHRqkS0mCszZk-eX5yWZAw0A130_head.
- 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.