Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- befree-2016 importedOn "2016-02-19" NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_assertion wasGeneratedBy ECO_0000203 NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_assertion wasDerivedFrom befree-2016 NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_assertion SIO_000772 17376794 NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_assertion evidence source_evidence_literature NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.
- NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_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." NP600337.RAj0cMLtO1aAHx1gEgND4LoNgqM1sWQYVn366Wzq1bc7c130_provenance.