Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP576873.RAw4TqZ6kF2zBDOKIqpZxOA-vOPzyR0tq0-Qc_aimig4E130_provenance.