Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_assertion> ?p ?o ?g. }
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- NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_assertion type Assertion NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_head.
- NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_assertion description "[The importance of a fully functional XPB is clearly illustrated by the severe clinical consequences associated with inherited defects in XPB including UV-hypersensitive syndromes xeroderma pigmentosum (XP), Cockayne syndrome (CS), combined XP and CS (XP/CS), and trichothiodystrophy (TTD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_provenance.
- NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_assertion evidence source_evidence_literature NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_provenance.
- NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_assertion SIO_000772 25641424 NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_provenance.
- NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_assertion wasDerivedFrom befree-2016 NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_provenance.
- NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_assertion wasGeneratedBy ECO_0000203 NP1260134.RAskLw7F3sRNkORoSRVwhDdpqi6GPq1cG9nMANjwSqYZk130_provenance.