Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_assertion type Assertion NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_head.
- NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_assertion description "[These new findings include rare germline mutations in other high penetrant genes, the most important of which include TP53 mutations in Li-Fraumeni syndrome, STK11 mutations in Peutz-Jeghers syndrome, and PTEN mutations in Cowden syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.
- NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_assertion evidence source_evidence_literature NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.
- NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_assertion SIO_000772 23586058 NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.
- NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_assertion wasDerivedFrom befree-20140225 NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.
- NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_assertion wasGeneratedBy ECO_0000203 NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.