Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_assertion> ?p ?o ?g. }
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- NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_assertion type Assertion NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_head.
- NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_assertion description "[Here, using low-coverage whole-genome sequencing of 5,303 Chinese women with recurrent MDD selected to reduce phenotypic heterogeneity, and 5,337 controls screened to exclude MDD, we identified, and subsequently replicated in an independent sample, two loci contributing to risk of MDD on chromosome 10: one near the SIRT1 gene (P?=?2.53?�?10(-10)), the other in an intron of the LHPP gene (P = 6.45?�?10(-12)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_provenance.
- NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_assertion evidence source_evidence_literature NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_provenance.
- NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_assertion SIO_000772 26176920 NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_provenance.
- NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_assertion wasDerivedFrom befree-2016 NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_provenance.
- NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_assertion wasGeneratedBy ECO_0000203 NP1290186.RAda9f1599e0Y1IHEXWDQI1vhU1JWjPZNzaoS8h-RJSgo130_provenance.