Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_assertion> ?p ?o ?g. }
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- NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_assertion type Assertion NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_head.
- NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_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." NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_provenance.
- NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_assertion evidence source_evidence_literature NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_provenance.
- NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_assertion SIO_000772 16421217 NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_provenance.
- NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_assertion wasDerivedFrom befree-20150227 NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_provenance.
- NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_assertion wasGeneratedBy ECO_0000203 NP381418.RASIJKZDDi1hfTVgwzxykT-SpXIXLFfAZiUHm0UKprnWY130_provenance.