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- source_evidence_literature type ECO_0000212 NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_assertion description "[This finding, and that of trisomy 7 and MET mutation in hereditary renal carcinoma represent the only cases of human tumors in which an increased number of chromosomes carrying an oncogene activated by point mutation have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_assertion evidence source_evidence_literature NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_assertion SIO_000772 10812167 NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_assertion wasDerivedFrom befree-20150227 NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_assertion wasGeneratedBy ECO_0000203 NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP803189.RAdRS-MqzrP61EPAgkLJ_SneaMPGWUdaT74SWYAe1uxm8130_provenance.