Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_assertion description "[To determine the role of the calcium-channel beta4-subunit gene CACNB4 on chromosome 2q22-23 in related human disorders, we screened for mutations in small pedigrees with familial epilepsy and ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_assertion evidence source_evidence_literature NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_assertion SIO_000772 10762541 NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_assertion wasDerivedFrom befree-20140225 NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_assertion wasGeneratedBy ECO_0000203 NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP241805.RAsaqa05sY5X5olCEPdW_EBlgMoenTK0fJLjHjjnJx5FY130_provenance.