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- source_evidence_literature type ECO_0000212 NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_assertion description "[In addition, rs3825885 (NTRK3, p�=�9�נ10(-4)) was identified as an AN risk variant, and rs11179027 (TPH2, p�=�2�נ10(-3)) as an OCD marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_assertion evidence source_evidence_literature NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_assertion SIO_000772 23337130 NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_assertion wasDerivedFrom befree-2016 NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_assertion wasGeneratedBy ECO_0000203 NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1045633.RAASJiTng5i9x4BB53Zzslw1DCNZTg_n4mZwucXXzbPxg130_provenance.