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- source_evidence_literature type ECO_0000212 NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_assertion description "[genotyping ALL patients for functional polymorphisms of candidate genes can become an important tool in predicting disease outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_assertion evidence source_evidence_literature NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_assertion SIO_000772 12041882 NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_assertion wasDerivedFrom gad-20150221 NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_assertion wasGeneratedBy ECO_0000203 NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP74515.RAhHboQUXv0SjLolEKeLfrEwR-SukR6RJs978ZtZZnVpk130_provenance.