Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion type Assertion NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_head.
- NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion description "[Autosomal recessive lissencephaly with cerebellar hypoplasia, accompanied by severe delay, hypotonia, and seizures, has been associated with mutations of the reelin (RELN) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_provenance.
- NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion evidence source_evidence_literature NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_provenance.
- NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion SIO_000772 15921228 NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_provenance.
- NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion wasDerivedFrom befree-20140225 NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_provenance.
- NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_assertion wasGeneratedBy ECO_0000203 NP547427.RAmjCI_x7k7I6Yn63FUh-bKfMjMbxsaXHnY_GtekLFIRs130_provenance.