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- NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_assertion type Assertion NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_head.
- NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_assertion description "[The full FMR-1 mutation is known to cause the fragile X syndrome [Fra(X)], but variable expression in females, including normal to deficient intellect, may be related to random X-inactivation (lyonization).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_provenance.
- NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_assertion evidence source_evidence_literature NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_provenance.
- NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_assertion SIO_000772 7943030 NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_provenance.
- NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_assertion wasDerivedFrom befree-2016 NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_provenance.
- NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_assertion wasGeneratedBy ECO_0000203 NP1327691.RAlzqb145VN7kv4G20ZBNYmkmkB2ag8yhFaQjyj1_pn9w130_provenance.