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- source_evidence_literature type ECO_0000212 NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_assertion description "[This study suggests a mechanism for the generation of different neuropsychiatric symptoms in AD from a single nucleotide polymorphism with reduced receptor binding in T102C 5-HT2A receptor gene homozygotes correlating with susceptibility to depressive symptoms, whereas the relative preservation of receptor binding in heterozygotes with AD correlating with susceptibility to hallucinations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_assertion evidence source_evidence_literature NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_assertion SIO_000772 17481814 NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_assertion wasDerivedFrom befree-20150227 NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_assertion wasGeneratedBy ECO_0000203 NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP471358.RAL-p00r9ROtk-6K14s7fMo8tUgcrIoWkdw1hG8WP1T9c130_provenance.