Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_assertion description "[While further work is needed to identify the actual functional genetic variants involved, these results suggest that a relationship exists between genetic variation in HTR2A and either 5-HTT expression or central serotonergic transmission that influences the therapeutic response to 5-HTT inhibition in major depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_assertion evidence source_evidence_literature NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_assertion SIO_000772 20047709 NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_assertion wasDerivedFrom befree-20140225 NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_assertion wasGeneratedBy ECO_0000203 NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP370878.RAme_n8OscFteBc6Kj9zygEVtzEUiAFA_0zV9Nt3sSZzQ130_provenance.