Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_assertion description "[We evaluated the OCTN1 and OCTN2 polymorphisms in 200 patients with UC, 59 patients with UCCP, 200 patients with SCC, and 200 controls (HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_assertion evidence source_evidence_literature NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_assertion SIO_000772 21793125 NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_assertion wasDerivedFrom befree-2016 NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_assertion wasGeneratedBy ECO_0000203 NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.
- befree-2016 importedOn "2016-02-19" NP912649.RA-UmwNc0w8WdmskRkvCYqFR-37UJ3oq49APzozCudHCA130_provenance.