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- source_evidence_literature type ECO_0000212 NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_assertion description "[Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_assertion evidence source_evidence_literature NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_assertion SIO_000772 25477152 NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_assertion wasDerivedFrom befree-2016 NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_assertion wasGeneratedBy ECO_0000203 NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245029.RAn77mM1oE6-9fK0xlD5pjK8IWvnNNFFEjnudtr5CRn0w130_provenance.