Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_assertion description "[Lissencephaly-pachygyria and subcortical band heterotopia (SBH) are disorders of neuronal migration and represent a malformative spectrum resulting from mutations of either LIS1 or DCX genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_assertion evidence source_evidence_literature NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_assertion SIO_000772 16724181 NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_assertion wasDerivedFrom befree-20150227 NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_assertion wasGeneratedBy ECO_0000203 NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP831652.RALXDCZkIR1k9ZFCT0C5zHLpu_0d-wYKxn2NCn9HhuGEA130_provenance.