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- NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_assertion type Assertion NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_head.
- NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_assertion wasGeneratedBy ECO_0000203 NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_provenance.
- NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_assertion wasDerivedFrom lhgdn-20090331 NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_provenance.
- NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_assertion SIO_000772 15492925 NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_provenance.
- NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_assertion evidence source_evidence_literature NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_provenance.
- NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_assertion description "[CDKL5 mutations are associated with epilepsy, X-linked mental retardation and a clinical phenotype that overlaps Rett syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207412.RA_AFrAQ7gK9Ij3eq3zJdDqOUatsq1pQJT-nwodDm97RE130_provenance.