Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_assertion wasGeneratedBy ECO_0000203 NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_assertion wasDerivedFrom befree-20150227 NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_assertion SIO_000772 17376794 NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_assertion evidence source_evidence_literature NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.
- NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_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." NP532034.RARNRKmHWk_B6UWNH7NJ4KfGh_Ietcx4BYqpEIa3pHKUQ130_provenance.