Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_assertion> ?p ?o ?g. }
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- NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_assertion type Assertion NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_head.
- NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_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." NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_provenance.
- NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_assertion evidence source_evidence_literature NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_provenance.
- NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_assertion SIO_000772 15921228 NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_provenance.
- NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_assertion wasDerivedFrom befree-20140225 NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_provenance.
- NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_assertion wasGeneratedBy ECO_0000203 NP921695.RAaGSC2u2l9loFu3lR5hZSX04VHRs_B3ppXaFPblctB4g130_provenance.