Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_assertion> ?p ?o ?g. }
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- NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_assertion type Assertion NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_head.
- NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_assertion wasGeneratedBy ECO_0000203 NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_provenance.
- NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_assertion wasDerivedFrom befree-20150227 NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_provenance.
- NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_assertion SIO_000772 10818218 NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_provenance.
- NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_assertion evidence source_evidence_literature NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_provenance.
- NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_assertion description "[The aim of this population screening study was to determine if Fra-X or FRAXE mutations are the cause of a number of cases of mental retardation in a sample of Mexican children with mental retardation of unknown cause (MRUC) and to stress the importance of performing molecular analysis of the FMR-1 gene in all patients with MRUC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412787.RAKD0_b_AcoQss_v00-UL0VRduIwlfADaRqT43z_5JgnE130_provenance.