Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_assertion description "[Subtle differences in the effects of these different mutations on the many activities of TFIIH and on its stability determine the clinical outcomes, which can be XP, TTD, XP with CS, XP with TTD or COFS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_assertion evidence source_evidence_literature NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_assertion SIO_000772 14726016 NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_assertion wasDerivedFrom befree-2016 NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_assertion wasGeneratedBy ECO_0000203 NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.
- befree-2016 importedOn "2016-02-19" NP428117.RAH3tN0Ovlrj1g8Elpsew-r1kWUHi4CkqtKhzg1XHYBHs130_provenance.