Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_assertion description "[In order to identify gene variants related to the serotonergic neurotransmitter system that possibly represent a hereditary risk factor for sporadic Alzheimer's disease (AD), patients suffering from AD and non-demented psychiatric inpatients without symptoms of dementia were genotyped for polymorphisms of HTR6 (267C/T) and HTR2A (-1438G/A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_assertion evidence source_evidence_literature NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_assertion SIO_000772 11725820 NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_assertion wasDerivedFrom befree-20140225 NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_assertion wasGeneratedBy ECO_0000203 NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP675714.RAwZMTn8WO9_zTy6EcMUJvTzq510h3_jTf0YjmD0tp8e0130_provenance.