Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_assertion type Assertion NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_head.
- NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_assertion description "[MECP2 mutations have also been identified in individuals with a variety of clinical syndromes, including mild learning-disability in females, neonatal encephalopathy in males, and psychiatric disorders, autism and X-linked mental retardation in both males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_provenance.
- NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_assertion evidence source_evidence_literature NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_provenance.
- NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_assertion SIO_000772 16647848 NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_provenance.
- NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_assertion wasDerivedFrom befree-2016 NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_provenance.
- NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_assertion wasGeneratedBy ECO_0000203 NP547446.RAJDrwUsraB9EIoRInNosxxxyXr9BzHWNSlIIygzBI-FY130_provenance.