Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_assertion> ?p ?o ?g. }
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- NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_assertion type Assertion NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_head.
- NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_assertion description "[Twenty-two cases with Turner syndrome features were subjected to standard cytogenetic techniques using giemsa trypsin (GTG-) banding then fluorescence in situ hybridization (FISH) using a specific whole-X chromosome painting probe, Quint-Essential Y-specific DNA probe (AMELY) for Yp11.2, alpha-satellite (DYZ3) probe and X/Y cocktail-alpha satellite probe (ONCOR) for confirmation of the initial diagnosis and comparison of the two techniques.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_provenance.
- NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_assertion evidence source_evidence_literature NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_provenance.
- NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_assertion SIO_000772 10738532 NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_provenance.
- NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_assertion wasDerivedFrom befree-20140225 NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_provenance.
- NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_assertion wasGeneratedBy ECO_0000203 NP660784.RADsT9s-q17Q7ZNtz-kjwp-63LiTcS9t_XaBCL-Pw7n-4130_provenance.