Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_assertion type Assertion NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_head.
- NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_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." NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_assertion evidence source_evidence_literature NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_assertion SIO_000772 15921228 NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_assertion wasDerivedFrom befree-20140225 NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_assertion wasGeneratedBy ECO_0000203 NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.