Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion> ?p ?o ?g. }
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- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion type Assertion NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_head.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_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." NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion evidence source_evidence_literature NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion SIO_000772 15921228 NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion wasDerivedFrom befree-20140225 NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.
- NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_assertion wasGeneratedBy ECO_0000203 NP356792.RABF7zywSwIqbklKR5hPAQbSPv1Ctm74Zwu38Fl0w25sw130_provenance.