Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_assertion> ?p ?o ?g. }
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- NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_assertion type Assertion NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_head.
- NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_provenance.
- NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_assertion evidence source_evidence_literature NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_provenance.
- NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_assertion SIO_000772 16235064 NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_provenance.
- NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_assertion wasDerivedFrom befree-20140225 NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_provenance.
- NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_assertion wasGeneratedBy ECO_0000203 NP256825.RAXZ12vYryOGiEp0vQnnV1B8IZjIc70H-ZcQvwa-fkSec130_provenance.