Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- befree-2016 importedOn "2016-02-19" NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_assertion wasGeneratedBy ECO_0000203 NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_assertion wasDerivedFrom befree-2016 NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_assertion SIO_000772 10767341 NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_assertion evidence source_evidence_literature NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.
- NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_assertion description "[Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281299.RAUk5yhcirMuadaaBc_1ne-RdVQ1LW1UhvoEB-EseNhLc130_provenance.