Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_assertion description "[Screening of the LGI4 coding region in BFIC and childhood absence epilepsy (CAE) revealed several frequent exonic polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_assertion evidence source_evidence_literature NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_assertion SIO_000772 14505228 NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_assertion wasDerivedFrom befree-20150227 NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_assertion wasGeneratedBy ECO_0000203 NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977408.RANvDCxJKMZjSyjkRbACbAe9oi4qBPFRFBE0sjVbsM2OY130_provenance.