Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_assertion description "[The rem mutations in the ATP-binding groove of the Rad3/XPD helicase lead to Xeroderma pigmentosum-Cockayne syndrome-like phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_assertion evidence source_evidence_literature NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_assertion SIO_000772 25500814 NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_assertion wasDerivedFrom befree-2016 NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_assertion wasGeneratedBy ECO_0000203 NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247406.RAuPxb4qa1v5UqQh-m37on3moIGBnOXfoqrZWxrHdNFaM130_provenance.