Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_assertion description "[A recent study suggested that a dodecamer duplication in exon 42 of the HOPA gene in Xq13 may be a significant factor in the etiology of X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_assertion evidence source_evidence_literature NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_assertion SIO_000772 10982179 NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_assertion wasDerivedFrom befree-20140225 NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_assertion wasGeneratedBy ECO_0000203 NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP165191.RAUgKGkWRNww2eArxRzNXekaY_z3elfgZJlRbVsf44VwY130_provenance.