Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_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." NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_assertion evidence source_evidence_literature NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_assertion SIO_000772 16421217 NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_assertion wasDerivedFrom befree-20140225 NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_assertion wasGeneratedBy ECO_0000203 NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP404347.RAYMWnBGz0SFxwxj-Kxf0Xdjtth_cU42UIyhS93IYjL6I130_provenance.