Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_assertion wasGeneratedBy ECO_0000203 NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_assertion wasDerivedFrom befree-20140225 NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_assertion SIO_000772 7550326 NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_assertion evidence source_evidence_literature NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_assertion description "[We have demonstrated the utility of this strategy in two different hereditary colorectal cancer syndromes, one caused by a defective tumour suppressor gene on chromosome 5 (familial adenomatous polyposis, FAP) and the other caused by a defective mismatch repair gene on chromosome 2 (hereditary non-polyposis colorectal cancer, HNPCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP900123.RAnI_8Y2CDhnxc-h_9-_r-WJeoBoGI6HFztxRFGi-uF_A130_provenance.