Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_assertion type Assertion NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_head.
- NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_assertion description "[Mutations in the ARX gene have been found in X-linked infantile spasms syndrome, Partington syndrome (mental retardation with dystonic movements of the hands), X-linked lissencephaly with abnormal genitalia, X-linked myoclonus epilepsy with spasticity and intellectual disability, and in nonsyndromic X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_provenance.
- NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_assertion evidence source_evidence_literature NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_provenance.
- NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_assertion SIO_000772 17641262 NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_provenance.
- NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_assertion wasDerivedFrom befree-2016 NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_provenance.
- NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_assertion wasGeneratedBy ECO_0000203 NP621055.RAJFVDfdq2PUe1ocSUJN2EGeJMZbaWbPPd1jGzmWL_LW0130_provenance.