Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_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." NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_assertion evidence source_evidence_literature NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_assertion SIO_000772 21793125 NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_assertion wasDerivedFrom befree-20140225 NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_assertion wasGeneratedBy ECO_0000203 NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP463729.RAKmMghNyNVjg__obV2HofDgsWZq2te-oe7B7Ksr_xJMU130_provenance.