Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_assertion> ?p ?o ?g. }
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- NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_assertion type Assertion NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_head.
- NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_assertion description "[Twenty children and young adults (age range 5 to 33 years, 12 females and eight males) with genetically confirmed 22q11 deletion syndrome (CATCH 22: Cardiac anomaly, Anomalous face, Thymus hypoplasia/aplasia, Cleft palate, and Hypocalcaemia), recruited from a large ongoing study, were given comprehensive assessments with a view to determining the pattern of neuropsychiatric and neuropsychological deficits thought to be part of the syndrome in many cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_provenance.
- NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_assertion evidence source_evidence_literature NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_provenance.
- NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_assertion SIO_000772 11811651 NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_provenance.
- NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_assertion wasDerivedFrom befree-2016 NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_provenance.
- NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_assertion wasGeneratedBy ECO_0000203 NP343279.RAAT4uRwJyJps9L_l05PoEr4a1Xq53oj2wAAlyp2v3UzQ130_provenance.