Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_assertion description "[Mutations in KCNT1 were found in two seemingly unrelated monogenic epilepsies including malignant migrating partial seizures of infancy and severe autosomal dominant nocturnal frontal lobe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_assertion evidence source_evidence_literature NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_assertion SIO_000772 23429546 NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_assertion wasDerivedFrom befree-20150227 NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_assertion wasGeneratedBy ECO_0000203 NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP932194.RAr8HAGsbEqkZcxd81i6nMqic6RwbRmOKPyJvxs19rVbI130_provenance.