Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_assertion type Assertion NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_head.
- NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_assertion description "[The fragile X mental retardation syndrome is caused by an expansion of a trinucleotide repeat (CGG)n in the FMR-1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_provenance.
- NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_assertion evidence source_evidence_literature NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_provenance.
- NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_assertion SIO_000772 7927336 NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_provenance.
- NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_assertion wasDerivedFrom befree-2016 NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_provenance.
- NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_assertion wasGeneratedBy ECO_0000203 NP1327256.RACQuV2mbT1dEnmbVOYCnEtRtONn-yyrsNlPILxX9-H-w130_provenance.