Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_assertion description "[Most patients with PCDH19 mutations exhibit a distinctive electroclinical pattern of focal seizures with affective symptoms, suggesting an epileptogenic dysfunction involving the frontotemporal limbic system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_assertion evidence source_evidence_literature NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_assertion SIO_000772 22946748 NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_assertion wasDerivedFrom befree-20140225 NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_assertion wasGeneratedBy ECO_0000203 NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477658.RAZgnEiJUyHR6jUNVHfeE1mvAxA_dnib0klQcLoE0nH_Q130_provenance.