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- source_evidence_literature type ECO_0000212 NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_assertion description "[To analyze whether genetic variants in the OXTR gene are associated with ASD we performed family-based single-marker and haplotype association analyses with 22 single nucleotide polymorphisms (SNPs) in the OXTR and its 5' region in 100 families with autistic disorders on high-functioning level (Asperger syndrome (AS), high-functioning autism (HFA), and atypical autism (AA)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_assertion evidence source_evidence_literature NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_assertion SIO_000772 19777562 NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_assertion wasDerivedFrom befree-2016 NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_assertion wasGeneratedBy ECO_0000203 NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.
- befree-2016 importedOn "2016-02-19" NP765113.RAxYLTyFsICXtxhQAJgrJ-OppLNag-kDZLl0yu6Riq0kk130_provenance.