Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_assertion> ?p ?o ?g. }
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- NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_assertion type Assertion NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_head.
- NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_assertion description "[This population was enriched in genes involved in cell migration, axonal guidance, neurogenesis, and regulation of transcription and includes genes implicated in autism, epilepsy, and mental retardation; all features recognized in patients with ARX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_provenance.
- NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_assertion evidence source_evidence_literature NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_provenance.
- NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_assertion SIO_000772 18799476 NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_provenance.
- NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_assertion wasDerivedFrom befree-20140225 NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_provenance.
- NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_assertion wasGeneratedBy ECO_0000203 NP644206.RAGl1CfXbx_C1lnLuHvGLGQDNCUzKwjm0rhTdHcz0vT-s130_provenance.