Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_assertion description "[Mutations in the DNA-dependent ATPase/helicase subunits of TFIIH, XPB and XPD, are associated with three inherited syndromes as follows: xeroderma pigmentosum with or without Cockayne syndrome and trichothiodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_assertion evidence source_evidence_literature NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_assertion SIO_000772 10660593 NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_assertion wasDerivedFrom befree-2016 NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_assertion wasGeneratedBy ECO_0000203 NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.
- befree-2016 importedOn "2016-02-19" NP274161.RAc1KskpVnDLBvTzfn7_mC0uXvgZseFN_YPLqy7JGLJr4130_provenance.