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- source_evidence_literature type ECO_0000212 NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_assertion description "[In male subjects, the variant rs6766410 (p.N163K) located in the HTR3C was significantly associated with OCD (p=0.007).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_assertion evidence source_evidence_literature NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_assertion SIO_000772 23928294 NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_assertion wasDerivedFrom befree-20150227 NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_assertion wasGeneratedBy ECO_0000203 NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978266.RAqhpxi9YlEdKgkFj6BO-di3knzPdpjpLrTcuBeZDWxoQ130_provenance.