Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_assertion description "[Three hundred and thirty nine healthy control participants (CON) and 179 participants clinically diagnosed with AT (TEN) from South Africa and Australia, were genotyped for variants: rs4143245, rs1249744, rs753085, rs946053 (COL27A1) and rs13321, rs2104772, rs1330363 (TNC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_assertion evidence source_evidence_literature NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_assertion SIO_000772 23192621 NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_assertion wasDerivedFrom befree-20140225 NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_assertion wasGeneratedBy ECO_0000203 NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485659.RAyb4mqlYbFns9qKc80ulFMg3JYZsYSB3N_5xAeGWstEQ130_provenance.