Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_assertion type Assertion NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_head.
- NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_assertion description "[The present study was designed to determine the frequency of germline mutations in the hMLH1 and hMSH2 genes in 31 families suspected of having hereditary nonpolyposis colorectal cancer who do not fulfill the criteria of the International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer but in whom a genetic basis for colon cancer is strongly suspected and 45 patients with sporadic early-onset colorectal cancer who developed colorectal cancer before the age of 40 years without any family history of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_provenance.
- NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_assertion evidence source_evidence_literature NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_provenance.
- NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_assertion SIO_000772 9559627 NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_provenance.
- NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_assertion wasDerivedFrom befree-2016 NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_provenance.
- NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_assertion wasGeneratedBy ECO_0000203 NP1393750.RA2I08PW5mhiS8V4OxQURZx3pRs2Hf6yff1L3r3lLrHII130_provenance.