Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_assertion description "[Therefore, the purpose of this study was to evaluate loss of heterozygosity (LOH) of 3p, APC, and p16 in a specific group of CUC-associated `adenoma-like` DALMs and to compare the results of this tumor with those in a well-defined group of CUC-associated non-adenoma-like DALMs and non-CUC-associated sporadic adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_assertion evidence source_evidence_literature NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_assertion SIO_000772 10976694 NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_assertion wasDerivedFrom befree-20140225 NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_assertion wasGeneratedBy ECO_0000203 NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP690013.RAGvl2XDskXelTzdETADyWou9iW7QpGRvV0aarDpRVG3A130_provenance.