Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion> ?p ?o ?g. }
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- NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion type Assertion NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_head.
- NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion description "[In summary, biallelic germline mutations of MYH are unlikely to cause colorectal cancer in patients sharing clinical features with hereditary nonpolyposis colorectal cancer families without mismatch repair defect and therefore cannot fill the molecular diagnostic gap in this subgroup of Bethesda-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_provenance.
- NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion evidence source_evidence_literature NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_provenance.
- NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion SIO_000772 16645203 NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_provenance.
- NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion wasDerivedFrom befree-20150227 NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_provenance.
- NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_assertion wasGeneratedBy ECO_0000203 NP580111.RAOScn8w0lRNdc1OecMV6Hyvj4AD6yqptud-OD0Rtynjo130_provenance.