Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_assertion description "[A second FHM3 mutation definitely established the epilepsy SCN1A gene as a migraine gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_assertion evidence source_evidence_literature NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_assertion SIO_000772 18451712 NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_assertion wasDerivedFrom befree-20140225 NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_assertion wasGeneratedBy ECO_0000203 NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP233421.RAM3IrK026DTz9MDsT8uNUsC44TLoL5Dm4laQkV1WVIIU130_provenance.