Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_assertion> ?p ?o ?g. }
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- NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_assertion type Assertion NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_head.
- NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_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." NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.
- NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_assertion evidence source_evidence_literature NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.
- NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_assertion SIO_000772 11725820 NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.
- NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_assertion wasDerivedFrom befree-2016 NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.
- NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_assertion wasGeneratedBy ECO_0000203 NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.