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- source_evidence_literature type ECO_0000212 NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_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." NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_assertion evidence source_evidence_literature NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_assertion SIO_000772 10762541 NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_assertion wasDerivedFrom befree-20150227 NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_assertion wasGeneratedBy ECO_0000203 NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP969120.RAEAu2HZwaSHIgA88qC_NWyg9xJFXw70JlYsDISiMqm7A130_provenance.