Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP337616.RAhlHNm1Z1qz90eihjCoFVqM6BMQf5AJRaKFji5Ytisdw130_provenance.