Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_assertion type Assertion NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_head.
- NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_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." NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_provenance.
- NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_assertion evidence source_evidence_literature NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_provenance.
- NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_assertion SIO_000772 7613092 NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_provenance.
- NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_assertion wasDerivedFrom befree-20140225 NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_provenance.
- NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_assertion wasGeneratedBy ECO_0000203 NP554626.RA9DQ9s-0FfzRNBBkzAlmj7jA_L-1lXbyatGy0L8BXbJ4130_provenance.