Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion> ?p ?o ?g. }
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- NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion type Assertion NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_head.
- NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion description "[To explore the hypothesis that this variability might result from the effects of differing combinations of overlooked variants within SLC6A4 together with small OCD and control sample sizes, we studied three common functional polymorphisms (5-HTTLPR, STin2, and the newly discovered SNP, rs25531) in the largest sample size of OCD patients (N=347) and controls (N=749) ever investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance.
- NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion evidence source_evidence_literature NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance.
- NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion SIO_000772 17375136 NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance.
- NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion wasDerivedFrom befree-2016 NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance.
- NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_assertion wasGeneratedBy ECO_0000203 NP600246.RA7HTLymia3X3QUb6_pUlK952xENZ_u5P1DbMYOqHshDs130_provenance.