Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_assertion> ?p ?o ?g. }
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- NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_assertion type Assertion NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_head.
- NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_assertion description "[In this study we used 1 Mb genome-wide array-CGH to screen 48 children with MR and congenital malformations for submicroscopic chromosomal imbalances, where the underlying cause was unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_provenance.
- NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_assertion evidence source_evidence_literature NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_provenance.
- NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_assertion SIO_000772 17901693 NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_provenance.
- NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_assertion wasDerivedFrom befree-2016 NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_provenance.
- NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_assertion wasGeneratedBy ECO_0000203 NP632351.RAzY_v1AMTVSUtxQgVXRFkdjTorLaCyXbvn07zKa4_7iE130_provenance.