Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_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." NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_assertion evidence source_evidence_literature NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_assertion SIO_000772 25641424 NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_assertion wasDerivedFrom befree-2016 NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_assertion wasGeneratedBy ECO_0000203 NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260135.RA7moqGMKiuLd40LueWdMCg27oZUOHFTguojJt9jXxtrU130_provenance.