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- source_evidence_literature type ECO_0000212 NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP539239.RAzaPBwywg6b6zmtGJqUu9nbzgtEzK5-MfpIVvlvbuNso130_provenance.