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- source_evidence_literature type ECO_0000212 NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_assertion description "[To test this hypothesis, we performed case-control analyses on all DNA polymorphic variation identified in a resequencing study of six candidate DCM genes (CSRP3, LDB3, MYH7, SCN5A, TCAP, and TNNT2) conducted in 289 unrelated white probands with DCM of unknown cause and 188 unrelated white controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_assertion evidence source_evidence_literature NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_assertion SIO_000772 20201937 NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_assertion wasDerivedFrom gad-20150221 NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_assertion wasGeneratedBy ECO_0000203 NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP121301.RAJ6mK98I_upjEurxu1V1rWfhksX148iM_yf6tCiSHAWA130_provenance.