Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_assertion type Assertion NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_head.
- NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_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." NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_provenance.
- NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_assertion evidence source_evidence_literature NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_provenance.
- NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_assertion SIO_000772 11725820 NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_provenance.
- NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_assertion wasDerivedFrom befree-20150227 NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_provenance.
- NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_assertion wasGeneratedBy ECO_0000203 NP471307.RAQUUANnJVQyO13d0VaVXJSfWXpURbPH8y88GRZtrxwUs130_provenance.