Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_assertion> ?p ?o ?g. }
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- NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_assertion type Assertion NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_head.
- NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_assertion description "[Cowden disease is an autosomal dominant disorder associated with an elevated risk of breast, thyroid and skin cancers, in which germline mutations of a tumour suppressor gene (PTEN) have been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_provenance.
- NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_assertion evidence source_evidence_literature NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_provenance.
- NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_assertion SIO_000772 10982030 NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_provenance.
- NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_assertion wasDerivedFrom befree-2016 NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_provenance.
- NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_assertion wasGeneratedBy ECO_0000203 NP294724.RABV3qTcTlscyQM1u5TryU9xItw3EYKWQM-vZkvFiuteE130_provenance.