Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_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." NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion evidence source_evidence_literature NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion SIO_000772 7550326 NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion wasDerivedFrom befree-20150227 NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion wasGeneratedBy ECO_0000203 NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.