Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_assertion description "[LS patients with MSH2 mutations are at an increased risk for not only UTUC but also BCa and could be offered appropriate screening.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_assertion evidence source_evidence_literature NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_assertion SIO_000772 22883484 NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_assertion wasDerivedFrom befree-2016 NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_assertion wasGeneratedBy ECO_0000203 NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1004336.RASm_DvFasnpIFQqEDaqE4tQGH82sQxrQsVkswQ8ig47E130_provenance.