Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion wasGeneratedBy ECO_0000203 NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion wasDerivedFrom gad-20150221 NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion SIO_000772 17376794 NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_assertion evidence source_evidence_literature NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.
- NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_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." NP82409.RAsp5SzLk9Z9H5dzBq42zhXcAW3Dw45uCeS39M4HbuYR8130_provenance.