Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_assertion description "[RAD (21,18,13) for all + RAD (X,Y) for cases with ultrasound abnormalities consistent with Turner syndrome + karyotyping for cases with ultrasound abnormalities seemed to be the best approach for the detection of chromosomal abnormalities when invasive prenatal testing is performed for diagnosis of thalassaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_assertion evidence source_evidence_literature NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_assertion SIO_000772 16421217 NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_assertion wasDerivedFrom befree-2016 NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_assertion wasGeneratedBy ECO_0000203 NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP531613.RArE8YcIiAayjLcycDxS7k4KGdCLXiz2PXaCIWkUJk7jQ130_provenance.