Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_assertion description "[Amniocentesis on a 32-year-old woman at risk for trisomy 21 by maternal serum triple screen showed a 46,Y,inv(X) (p22.1q24) karyotype in all cells analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_assertion evidence source_evidence_literature NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_assertion SIO_000772 10588841 NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_assertion wasDerivedFrom befree-20140225 NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_assertion wasGeneratedBy ECO_0000203 NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.
- befree-20140225 importedOn "2014-02-25" NP559995.RApB_zoIkFYy3IDQeb8HLxmm1238fv32QYtEzbJnw8a2c130_provenance.