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- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion type Assertion NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_head.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion wasGeneratedBy ECO_0000203 NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion wasDerivedFrom befree-20150227 NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion SIO_000772 7550326 NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_provenance.
- NP394730.RAd4nMz33NkptVYh4LfDVimrHoFU197k8OYKagm9IWxCI130_assertion evidence source_evidence_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.