Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion> ?p ?o ?g. }
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- NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion type Assertion NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_head.
- NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion description "[When using array CGH to identify the cause for mental retardation in a 7-year-old child we found a submicroscopic de novo deletion of chromosome 17p13.1, which includes several genes likely to be causative for her phenotype, and also of TP53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_provenance.
- NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion evidence source_evidence_literature NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_provenance.
- NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion SIO_000772 19269943 NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_provenance.
- NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion wasDerivedFrom befree-20150227 NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_provenance.
- NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_assertion wasGeneratedBy ECO_0000203 NP750734.RAYSHP6WsHeMbFASeqPWTsUdSdFi-jyJFieMTpP2-ffRY130_provenance.