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- source_evidence_literature type ECO_0000212 NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_assertion description "[Mood disorder subjects (N=191) and healthy volunteers (N=125), all Caucasian subjects of European origin, were genotyped for the triallelic 5-HTTLPR polymorphism (higher expressing allele: L(A); lower expressing alleles: L(G), S).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_assertion evidence source_evidence_literature NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_assertion SIO_000772 16946185 NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_assertion wasDerivedFrom befree-2016 NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_assertion wasGeneratedBy ECO_0000203 NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.
- befree-2016 importedOn "2016-02-19" NP566992.RAg1MzxfDNKC4AZb1U7ShBEFEPlCunebwe3kUS_kn_82E130_provenance.