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- NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_assertion type Assertion NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_head.
- NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_assertion wasGeneratedBy ECO_0000203 NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_provenance.
- NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_assertion wasDerivedFrom befree-2016 NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_provenance.
- NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_assertion SIO_000772 17084570 NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_provenance.
- NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_assertion evidence source_evidence_literature NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_provenance.
- NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_assertion description "[Mutations in MECP2 gene, located in Xq28, have been reported as being the major cause of Rett syndrome and are also associated with some cases of X-linked mental retardation in both males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP577753.RAOXKINO2eBSjZ-1-zb_QCpNTgf_FU1Tx45gP-5YB0_5w130_provenance.