Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_assertion description "[High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_assertion evidence source_evidence_literature NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_assertion SIO_000772 19401682 NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_assertion wasDerivedFrom gad-20130706 NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_assertion wasGeneratedBy ECO_0000203 NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.
- gad-20130706 importedOn "2013-07-06" NP78713.RAl3qP92QwgB1ABN53uYav56sJxFa2Tk09e3JT2RJSlNc130_provenance.