Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_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." NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_assertion evidence source_evidence_literature NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_assertion SIO_000772 15921228 NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_assertion wasDerivedFrom befree-2016 NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_assertion wasGeneratedBy ECO_0000203 NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.
- befree-2016 importedOn "2016-02-19" NP496784.RApMwda4gJtUdqw65AiG0t76OpHjmGO24IcbQXGG5PScw130_provenance.