Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_assertion type Assertion NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_head.
- NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_assertion description "[The dysfunction of TFIIH could result in a large panel of genetic disorders, such as xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_provenance.
- NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_assertion evidence source_evidence_literature NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_provenance.
- NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_assertion SIO_000772 7613092 NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_provenance.
- NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_assertion wasDerivedFrom befree-20150227 NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_provenance.
- NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_assertion wasGeneratedBy ECO_0000203 NP1011260.RAKI0XbVzJSJAl_okew1wgWf_dMcQpz0US5aWs2iyvXEk130_provenance.