Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion> ?p ?o ?g. }
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- NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion type Assertion NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_head.
- NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion description "[Inherited mutations in the XPD subunit of the general transcription/repair factor TFIIH yield the rare genetic disorder Xeroderma pigmentosum (XP), the phenotypes of which cannot be explained solely on the basis of a DNA repair defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_provenance.
- NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion evidence source_evidence_literature NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_provenance.
- NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion SIO_000772 11955452 NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_provenance.
- NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion wasDerivedFrom befree-2016 NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_provenance.
- NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_assertion wasGeneratedBy ECO_0000203 NP351889.RAfw2eZ7vJrYWJLc4SmcRLQATGN8TdIsIxE-iPnE4RYMM130_provenance.