Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_assertion description "[Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_assertion evidence source_evidence_literature NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_assertion SIO_000772 11810107 NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_assertion wasDerivedFrom befree-2016 NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_assertion wasGeneratedBy ECO_0000203 NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.
- befree-2016 importedOn "2016-02-19" NP343216.RAfrjwyg0h4xRzKiARg1ZaEBQ7pkiThr8z2LgucL0q6N8130_provenance.