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- source_evidence_literature type ECO_0000212 NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_assertion description "[Cognitive correlates of a functional COMT polymorphism in children with 22q11.2 deletion syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_assertion evidence source_evidence_literature NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_assertion SIO_000772 16542388 NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_assertion wasDerivedFrom befree-2016 NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_assertion wasGeneratedBy ECO_0000203 NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.
- befree-2016 importedOn "2016-02-19" NP540685.RAm1M0yd4OLXZFQm8UV551GeLs9gi1tuJjn-IMiAuCjAk130_provenance.