Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion> ?p ?o ?g. }
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- NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion type Assertion NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_head.
- NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion description "[Nominally significant single SNP and/or haplotype-based association results were detected in 15 genes, of which, MYO1D, ACCN1 and LASP1 stand out as genes with autism risk alleles requiring further study, with potential GRRs in the range of 1.34-2.29.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_provenance.
- NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion evidence source_evidence_literature NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_provenance.
- NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion SIO_000772 17376794 NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_provenance.
- NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion wasDerivedFrom befree-2016 NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_provenance.
- NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_assertion wasGeneratedBy ECO_0000203 NP600336.RAAi70XkRM6XF3oOaGXpKboe-bLLs2Z1l2J5tga-bvcLQ130_provenance.