Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_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." NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_assertion evidence source_evidence_literature NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_assertion SIO_000772 16724181 NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_assertion wasDerivedFrom befree-20150227 NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_assertion wasGeneratedBy ECO_0000203 NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP649681.RAGsAcaC15B1yX0n9NmizwFRdYKcOSWQMAoQ8xustFXVk130_provenance.