Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion type Assertion NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_head.
- NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_provenance.
- NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion evidence source_evidence_literature NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_provenance.
- NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion SIO_000772 10660593 NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_provenance.
- NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion wasDerivedFrom befree-2016 NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_provenance.
- NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_assertion wasGeneratedBy ECO_0000203 NP274169.RA_UhEIXMV37JYynzTNwpybYh3625DZoRdNShq8neeDrg130_provenance.