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- NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_assertion type Assertion NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_head.
- NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_assertion wasGeneratedBy ECO_0000203 NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_provenance.
- NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_assertion wasDerivedFrom befree-2016 NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_provenance.
- NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_assertion SIO_000772 10818218 NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_provenance.
- NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_assertion evidence source_evidence_literature NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_provenance.
- NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_assertion description "[Our findings confirm that the molecular analysis of the FMR-1 gene is necessary in MRUC patients to achieve unequivocal diagnosis of fragile X syndrome, carrier premutation detection and for accurate genetic counseling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284419.RAY0FiIzTrDTaY5e4o4kBrkK0XQFkUsEVsBg2MkccHCxc130_provenance.