Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_assertion> ?p ?o ?g. }
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- NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_assertion type Assertion NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_head.
- NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_assertion description "[Fragile X syndrome (FXS) is caused by a full mutation expansion (>200 CGG repeats) in the FMR1 gene that results in a deficiency of the fragile X mental retardation protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_provenance.
- NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_assertion evidence source_evidence_literature NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_provenance.
- NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_assertion SIO_000772 16685180 NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_provenance.
- NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_assertion wasDerivedFrom befree-2016 NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_provenance.
- NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_assertion wasGeneratedBy ECO_0000203 NP548891.RAvMEJoQib1ImFalIPNyADQgRo-GbmwRqCjVC7RKQ-9t4130_provenance.