Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_assertion description "[GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_assertion evidence source_evidence_literature NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_assertion SIO_000772 23933820 NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_assertion wasDerivedFrom befree-20140225 NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_assertion wasGeneratedBy ECO_0000203 NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP533304.RAWgnbdV230JBjbFvF9j5QJ7qBCzL4gC5cBos9zEs4SUI130_provenance.