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- source_evidence_literature type ECO_0000212 NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_assertion description "[Since NE signaling contributes to diverse brain functions, we hypothesize that promoter variation within the human NET gene (solute carrier family 6, member 2; SLC6A2) may impact risk for NE-related disorders, including depression, attention deficit hyperactive disorder (ADHD), and autonomic dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_assertion evidence source_evidence_literature NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_assertion SIO_000772 18591486 NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_assertion wasDerivedFrom befree-20150227 NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_assertion wasGeneratedBy ECO_0000203 NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.
- befree-20150227 importedOn "2015-02-27" NP697961.RAUrbtaJypewmhkS8uIWiUkx1LSr2DL_CmvxOabaAL26k130_provenance.