Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_assertion> ?p ?o ?g. }
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- NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_assertion type Assertion NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_head.
- NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_assertion description "[Aristaless-related homeobox (ARX) gene mutations cause a diverse spectrum of disorders of the human brain, including lissencephaly, various forms of epilepsy and non-syndromic mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_provenance.
- NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_assertion evidence source_evidence_literature NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_provenance.
- NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_assertion SIO_000772 19738637 NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_provenance.
- NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_assertion wasDerivedFrom befree-2016 NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_provenance.
- NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_assertion wasGeneratedBy ECO_0000203 NP762181.RAzXM4JCsXr1PL0wroNC8hxc7_Uhsarf2xzCq-F24sj2E130_provenance.