Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- befree-2016 importedOn "2016-02-19" NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_assertion wasGeneratedBy ECO_0000203 NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_assertion wasDerivedFrom befree-2016 NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_assertion SIO_000772 19191227 NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_assertion evidence source_evidence_literature NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.
- NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_assertion description "[LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718519.RAhSiedSsNmY4jgRoF2R10M3i5ms0AcBT9I0tTYj_AH18130_provenance.