Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_assertion wasGeneratedBy ECO_0000203 NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_assertion wasDerivedFrom lhgdn-20090331 NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_assertion SIO_000772 19139306 NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_assertion evidence source_evidence_literature NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.
- NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_assertion description "[We broadened the clinical spectrum associated with SLC1A3 mutations to include milder manifestations of EA without seizures or alternating hemiplegia/severity of EA6 symptoms is related to the extent of glutamate transporter dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP244934.RAR-04RzZOBKkB-M7EvZu9EZ2P37YbG798MheeZK5py_E130_provenance.