Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_assertion wasGeneratedBy ECO_0000203 NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_assertion wasDerivedFrom befree-20140225 NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_assertion SIO_000772 21844054 NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_assertion evidence source_evidence_literature NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_assertion description "[Dravet syndrome is a rare epileptic encephalopathy linked to mutations in SCN1A (neuronal sodium channel α1 subunit) and characterized by an onset in infancy with polymorphous seizure types and developmental decline.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP804995.RAUw3508w8feRwOTZPGFy4pO6B_UNVGLm-LjaJ9dZQcfQ130_provenance.