Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_assertion> ?p ?o ?g. }
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- NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_assertion type Assertion NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_head.
- NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_assertion description "[To analyze whether genetic variants in the OXTR gene are associated with ASD we performed family-based single-marker and haplotype association analyses with 22 single nucleotide polymorphisms (SNPs) in the OXTR and its 5' region in 100 families with autistic disorders on high-functioning level (Asperger syndrome (AS), high-functioning autism (HFA), and atypical autism (AA)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_provenance.
- NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_assertion evidence source_evidence_literature NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_provenance.
- NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_assertion SIO_000772 19777562 NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_provenance.
- NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_assertion wasDerivedFrom befree-2016 NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_provenance.
- NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_assertion wasGeneratedBy ECO_0000203 NP765112.RAb57NXPmiyk_uDEilSkGgU-eXdRatBUgrWsyX_h7Zwkw130_provenance.