Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_assertion type Assertion NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_head.
- NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_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." NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_provenance.
- NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_assertion evidence source_evidence_literature NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_provenance.
- NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_assertion SIO_000772 16421217 NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_provenance.
- NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_assertion wasDerivedFrom befree-20140225 NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_provenance.
- NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_assertion wasGeneratedBy ECO_0000203 NP477389.RATYaxNPjFmtDVrSVywbHVAKPbT6LcRhuNKUleoZz_ib4130_provenance.